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Human (GRCh38.p14)
Description

high mobility group nucleosomal binding domain 2 [Source:HGNC Symbol;Acc:HGNC:4986]

Gene Synonyms

HMG17

Location
About this transcript

This transcript has 6 exons, is annotated with 15 domains and features, is associated with 2728 variant alleles and maps to 566 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000361427.6HMGN2-201194090aaENSP00000355228.5
 
Protein coding
CCDS283P05204 NM_005517.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000718304.1HMGN2-210350790aaENSP00000520737.1
 
Protein coding
CCDS283--GENCODE BasicAPPRIS P1
ENST00000493418.1HMGN2-2091496No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000460563.5HMGN2-2021045No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000479815.5HMGN2-2081030No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000466194.1HMGN2-205952No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000467700.5HMGN2-206932No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000463817.5HMGN2-203853No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000464888.5HMGN2-204565No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000468388.5HMGN2-207320No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 6, Coding exons: 6, Transcript length: 1,940 bps, Translation length: 90 residues

MANE

This MANE Select transcript contains ENSP00000355228 and matches to NM_005517.4 and NP_005508.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P05204

CCDS

This transcript is a member of the Human CCDS set: CCDS283

Transcript Support Level (TSL)

TSL:1

Version

ENST00000361427.6

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.

GENCODE primary gene

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