Human (GRCh38.p14)
Description

even-skipped homeobox 1 [Source:HGNC Symbol;Acc:HGNC:3506]

Location
About this transcript

This transcript has 3 exons, is annotated with 20 domains and features, is associated with 3166 variant alleles and maps to 460 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000496902.7EVX1-2022858407aaENSP00000419266.3
 
Protein coding
CCDS5413P49640-1 NM_001989.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000580535.1EVX1-2041635106aaENSP00000463759.1
 
Protein coding
J3QQJ1 -TSL:2CDS 5' incomplete
ENST00000222761.7EVX1-2011500201aaENSP00000222761.3
 
Protein coding
F8W9J5 -GENCODE basicTSL:1
ENST00000518886.1EVX1-203380No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 3, Coding exons: 3, Transcript length: 2,858 bps, Translation length: 407 residues

MANE

This MANE Select transcript contains ENSP00000419266 and matches to NM_001989.5 and NP_001980.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P49640

CCDS

This transcript is a member of the Human CCDS set: CCDS5413

Transcript Support Level (TSL)

TSL:1

Version

ENST00000496902.7

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.