Human (GRCh38.p14)
Description

coagulation factor XII [Source:HGNC Symbol;Acc:HGNC:3530]

Location

Chromosome 5: 177,402,133-177,416,583 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 12 transcripts (splice variants), 185 orthologues, 16 paralogues and is associated with 7 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000253496.4F12-2012036615aaENSP00000253496.3
 
Protein coding
CCDS34302P00748 NM_000505.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000696201.1F12-2121917578aaENSP00000512482.1
 
Protein coding
A0A8Q3WL25 -GENCODE basic
ENST00000696193.1F12-208258047aaENSP00000512477.1
 
Nonsense mediated decay
A0A8Q3WL28 --
ENST00000696192.1F12-2072295193aaENSP00000512476.1
 
Nonsense mediated decay
A0A8Q3WL37 --
ENST00000696194.1F12-2092224194aaENSP00000512478.1
 
Nonsense mediated decay
A0A8Q3WL35 --
ENST00000514943.1F12-206429No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000696195.1F12-2104830No protein-
 
Retained intron
---
ENST00000696200.1F12-2112351No protein-
 
Retained intron
---
ENST00000510358.5F12-2051573No protein-
 
Retained intron
--TSL:2
ENST00000502854.5F12-2021480No protein-
 
Retained intron
--TSL:5
ENST00000504406.5F12-204943No protein-
 
Retained intron
--TSL:2
ENST00000503736.1F12-203748No protein-
 
Retained intron
--TSL:3