Human (GRCh38.p14)
Description

meprin A subunit alpha [Source:HGNC Symbol;Acc:HGNC:7015]

Gene Synonyms

PPHA

Location
About this transcript

This transcript has 14 exons, is annotated with 56 domains and features, is associated with 21637 variant alleles and maps to 553 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000230588.9MEP1A-2012893746aaENSP00000230588.4
 
Protein coding
CCDS4918Q16819 NM_005588.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000611727.2MEP1A-2022363774aaENSP00000480465.1
 
Protein coding
B7ZL91 -GENCODE basicTSL:1
ENST00000680229.1MEP1A-2032301278aaENSP00000505289.1
 
Nonsense mediated decay
A0A7P0Z478 --
ENST00000680769.1MEP1A-2042441No protein-
 
Retained intron
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Statistics

Exons: 14, Coding exons: 14, Transcript length: 2,893 bps, Translation length: 746 residues

MANE

This MANE Select transcript contains ENSP00000230588 and matches to NM_005588.3 and NP_005579.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q16819

CCDS

This transcript is a member of the Human CCDS set: CCDS4918

Transcript Support Level (TSL)

TSL:1

Version

ENST00000230588.9

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.