Human (GRCh38.p14)
Description

PR/SET domain 7 [Source:HGNC Symbol;Acc:HGNC:9351]

Gene Synonyms

ZNF910

Location
About this transcript

This transcript has 11 exons, is annotated with 17 domains and features, is associated with 9559 variant alleles and maps to 452 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000449207.8PRDM7-2023393492aaENSP00000396732.2
 
Protein coding
CCDS45557Q9NQW5-3 NM_001098173.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000564210.2PRDM7-20371473aaENSP00000457667.1
 
Nonsense mediated decay
H3BUJ3 -TSL:5
ENST00000568473.5PRDM7-204706138aaENSP00000455390.1
 
Nonsense mediated decay
A4Q9G9 -TSL:5
ENST00000569206.1PRDM7-205693No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000325921.10PRDM7-2012442No protein-
 
Retained intron
--TSL:1
Statistics

Exons: 11, Coding exons: 10, Transcript length: 3,393 bps, Translation length: 492 residues

MANE

This MANE Select transcript contains ENSP00000396732 and matches to NM_001098173.2 and NP_001091643.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NQW5

CCDS

This transcript is a member of the Human CCDS set: CCDS45557

Transcript Support Level (TSL)

TSL:1

Version

ENST00000449207.8

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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