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Human (GRCh38.p14)
Description

male germ cell associated kinase [Source:HGNC Symbol;Acc:HGNC:6816]

Gene Synonyms

DJ417M14.2, RP62

Location
About this transcript

This transcript has 15 exons, is annotated with 18 domains and features, is associated with 32605 variant alleles and maps to 556 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000354489.7MAK-2023942648aaENSP00000346484.3
 
Protein coding
CCDS75399P20794-2 NM_001242957.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P4TSL:5
ENST00000313243.6MAK-2013984623aaENSP00000313021.2
 
Protein coding
CCDS4516P20794-1 -GENCODE BasicAPPRIS ALT1TSL:5
ENST00000474039.5MAK-2033859623aaENSP00000476067.1
 
Protein coding
CCDS4516P20794-1 -GENCODE PrimaryGENCODE BasicAPPRIS ALT1TSL:1
ENST00000536370.6MAK-2043736583aaENSP00000442221.2
 
Protein coding
CCDS75398P20794-3 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000676116.1MAK-2073343549aaENSP00000502045.1
 
Protein coding
CCDS93855A0A6Q8PG01 -GENCODE PrimaryGENCODE Basic
ENST00000675026.1MAK-2062668501aaENSP00000502542.1
 
Nonsense mediated decay
A0A6Q8PH30 --
ENST00000538030.3MAK-2052508457aaENSP00000442250.1
 
Nonsense mediated decay
Q8IXN4 -TSL:1
Statistics

Exons: 15, Coding exons: 14, Transcript length: 3,942 bps, Translation length: 648 residues

MANE

This MANE Select transcript contains ENSP00000346484 and matches to NM_001242957.3 and NP_001229886.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P20794

CCDS

This transcript is a member of the Human CCDS set: CCDS75399

Transcript Support Level (TSL)

TSL:5

Version

ENST00000354489.7

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.

Annotation Attributes

CAGE supported TSS [Definitions]

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.