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Human (GRCh37.p13)
Description

ATPase, Ca++ transporting, plasma membrane 2 [Source:HGNC Symbol;Acc:815]

Gene Synonyms

PMCA2, PMCA2a, PMCA2i

Location

Chromosome 3: 10,365,707-10,749,716 reverse strand.

GRCh37:CM000665.1

About this gene

This gene has 10 transcripts (splice variants), 3 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000360273.2ATP2B2-20289621243aaENSP00000353414.2
 
Protein coding
CCDS33701Q01814 Q4J696 Q4J699
NM_001001331.2Ensembl CanonicalGENCODE basic
ENST00000397077.1ATP2B2-00589641198aaENSP00000380267.1
 
Protein coding
CCDS2601Q01814 Q4LE63 -GENCODE basic
ENST00000343816.4ATP2B2-20189201229aaENSP00000344677.4
 
Protein coding
Q01814 Q4J696 -GENCODE basic
ENST00000383800.4ATP2B2-00289001198aaENSP00000373311.4
 
Protein coding
CCDS2601Q01814 Q4LE63 NM_001683.3GENCODE basic
ENST00000352432.4ATP2B2-00185931243aaENSP00000324172.5
 
Protein coding
CCDS33701Q01814 Q4J696 Q4J699
-GENCODE basic
ENST00000452124.1ATP2B2-00340161099aaENSP00000414854.1
 
Protein coding
H0Y7S3 -CDS 5' incomplete
ENST00000460129.1ATP2B2-00491011154aaENSP00000424494.1
 
Nonsense mediated decay
Q01814 --
ENST00000467702.2ATP2B2-006907No protein-
 
Processed transcript
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ENST00000468426.1ATP2B2-009496No protein-
 
Processed transcript
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ENST00000480680.2ATP2B2-0081739No protein-
 
Retained intron
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