Human (GRCh38.p14)
Description

egl-9 family hypoxia inducible factor 1 [Source:HGNC Symbol;Acc:HGNC:1232]

Gene Synonyms

C1ORF12, HIFPH2, PHD2, SM-20, ZMYND6

About this transcript

This transcript has 5 exons, is annotated with 90 domains and features, is associated with 26913 variant alleles and maps to 715 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000366641.4EGLN1-2014335426aaENSP00000355601.3
 
Protein coding
CCDS1595Q9GZT9-1 NM_022051.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000667629.1EGLN1-2063108113aaENSP00000499629.1
 
Protein coding
A0A590UJZ0 -CDS 5' incomplete
ENST00000658954.1EGLN1-2041090175aaENSP00000499299.1
 
Protein coding
A0A590UJ78 -CDS 5' incomplete
ENST00000670301.1EGLN1-20778381aaENSP00000499368.1
 
Protein coding
A0A590UJD6 -CDS 5' incomplete
ENST00000654803.1EGLN1-2031525159aaENSP00000499591.1
 
Nonsense mediated decay
A0A590UJT7 -CDS 5' incomplete
ENST00000476717.2EGLN1-202614No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000663780.1EGLN1-205570No protein-
 
Retained intron
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Statistics

Exons: 5, Coding exons: 5, Transcript length: 4,335 bps, Translation length: 426 residues

MANE

This MANE Select transcript contains ENSP00000355601 and matches to NM_022051.3 and NP_071334.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9GZT9

CCDS

This transcript is a member of the Human CCDS set: CCDS1595

Transcript Support Level (TSL)

TSL:1

Version

ENST00000366641.4

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.