Human (GRCh38.p14)
Description

transferrin [Source:HGNC Symbol;Acc:HGNC:11740]

Gene Synonyms

PRO1557, PRO2086

Location

Chromosome 3: 133,746,040-133,796,641 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 14 transcripts (splice variants), 170 orthologues, 3 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000402696.9TF-20120166698aaENSP00000385834.3
 
Protein coding
CCDS3080P02787 NM_001063.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000482271.5TF-210659134aaENSP00000419338.1
 
Protein coding
C9JVG0 -TSL:4CDS 3' incomplete
ENST00000466911.5TF-20652675aaENSP00000417468.1
 
Protein coding
C9JB55 -TSL:4CDS 3' incomplete
ENST00000461695.1TF-204990143aaENSP00000419714.1
 
Nonsense mediated decay
H7C5E8 -TSL:3CDS 5' incomplete
ENST00000494430.5TF-213594120aaENSP00000418396.1
 
Nonsense mediated decay
F8WCI6 -TSL:4
ENST00000485977.1TF-211580102aaENSP00000418716.1
 
Nonsense mediated decay
F8WC57 -TSL:3
ENST00000414694.5TF-202546115aaENSP00000401505.1
 
Nonsense mediated decay
F8WEK9 -TSL:4
ENST00000475382.5TF-209586No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000467842.1TF-2074602No protein-
 
Retained intron
--TSL:1
ENST00000493011.5TF-212999No protein-
 
Retained intron
--TSL:2
ENST00000498622.1TF-214719No protein-
 
Retained intron
--TSL:2
ENST00000474287.5TF-208645No protein-
 
Retained intron
--TSL:2
ENST00000462495.1TF-205582No protein-
 
Retained intron
--TSL:2
ENST00000460531.5TF-203577No protein-
 
Retained intron
--TSL:4