Human (GRCh38.p14)
Description

coagulation factor VII [Source:HGNC Symbol;Acc:HGNC:3544]

Location

Chromosome 13: 113,105,788-113,120,685 forward strand.

GRCh38:CM000675.2

About this gene

This gene has 6 transcripts (splice variants), 274 orthologues, 16 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000346342.8F7-2013063444aaENSP00000329546.4
 
Protein coding
CCDS9529P08709-2 NM_019616.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000375581.3F7-2023109466aaENSP00000364731.3
 
Protein coding
CCDS9528P08709-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000541084.5F7-2062873382aaENSP00000442051.2
 
Protein coding
CCDS73602F5H8B0 -GENCODE basicTSL:2
ENST00000444337.1F7-20356474aaENSP00000387669.1
 
Nonsense mediated decay
E9PH36 -TSL:5
ENST00000473085.1F7-204558No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000479674.1F7-205767No protein-
 
Retained intron
--TSL:5