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Human (GRCh38.p14)
Description

5-hydroxymethylcytosine binding, ES cell specific [Source:HGNC Symbol;Acc:HGNC:24446]

Gene Synonyms

C3ORF37, DC12, SRAPD1

About this transcript

This transcript has 7 exons, is annotated with 15 domains and features, is associated with 11254 variant alleles and maps to 391 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000383463.9HMCES-2012485354aaENSP00000372955.3
 
Protein coding
CCDS33852Q96FZ2 NM_020187.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000502878.6HMCES-2041952354aaENSP00000426215.1
 
Protein coding
CCDS33852Q96FZ2 -GENCODE BasicAPPRIS P1TSL:1
ENST00000389735.7HMCES-2021763354aaENSP00000374385.3
 
Protein coding
CCDS33852Q96FZ2 -GENCODE BasicAPPRIS P1TSL:1
ENST00000417226.6HMCES-2031490312aaENSP00000392966.2
 
Protein coding
CCDS87134E7EMP6 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000509042.5HMCES-205948282aaENSP00000423132.1
 
Protein coding
D6R9T3 -TSL:3CDS 3' incomplete
ENST00000509551.5HMCES-206774233aaENSP00000424594.1
 
Protein coding
D6RAZ3 -TSL:5CDS 3' incomplete
ENST00000511665.1HMCES-208643140aaENSP00000421895.1
 
Protein coding
D6RAI0 -TSL:5CDS 3' incomplete
ENST00000510314.5HMCES-207599183aaENSP00000426276.1
 
Protein coding
D6RGK7 -TSL:5CDS 3' incomplete
Statistics

Exons: 7, Coding exons: 6, Transcript length: 2,485 bps, Translation length: 354 residues

MANE

This MANE Select transcript contains ENSP00000372955 and matches to NM_020187.3 and NP_064572.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96FZ2

CCDS

This transcript is a member of the Human CCDS set: CCDS33852

Transcript Support Level (TSL)

TSL:1

Version

ENST00000383463.9

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.