Human (GRCh38.p14)
Description

solute carrier family 28 member 2 [Source:HGNC Symbol;Acc:HGNC:11002]

Gene Synonyms

CNT2, HCNT2, HST17153, SPNT1

Location

Chromosome 15: 45,252,234-45,277,846 forward strand.

GRCh38:CM000677.2

About this gene

This gene has 4 transcripts (splice variants), 197 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000347644.8SLC28A2-2014371658aaENSP00000315006.4
 
Protein coding
CCDS10121O43868 NM_004212.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000560438.5SLC28A2-203581193aaENSP00000454074.1
 
Protein coding
H0YNM6 -TSL:4CDS 5' and 3' incomplete
ENST00000559924.1SLC28A2-20276971aaENSP00000454046.1
 
Nonsense mediated decay
H0YNK4 -TSL:5CDS 5' incomplete
ENST00000560767.1SLC28A2-2041567No protein-
 
Protein coding CDS not defined
--TSL:2