Human (GRCh38.p14)
Description

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

About this transcript

This transcript has 8 exons, is annotated with 43 domains and features, is associated with 9821 variant alleles and maps to 474 oligo probes.

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
Statistics

Exons: 8, Coding exons: 8, Transcript length: 3,063 bps, Translation length: 444 residues

MANE

This MANE Select transcript contains ENSP00000329546 and matches to NM_019616.4 and NP_062562.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P08709

CCDS

This transcript is a member of the Human CCDS set: CCDS9529

Transcript Support Level (TSL)

TSL:1

Version

ENST00000346342.8

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.