Canonical Allele Identifier: CA343952653
Gene: PLA2G4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186956308T>G , CM000663.2:g.186956308T>G GRCh38
NC_000001.10:g.186925440T>G , CM000663.1:g.186925440T>G GRCh37
NC_000001.9:g.185192063T>G NCBI36
NG_012203.1:g.132409T>G
NG_012203.2:g.132409T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.1543T>G MANE Select ENSP00000356436.3:p.Ser515Ala
ENST00000367466.3:c.1543T>G ENSP00000356436.3:p.Ser515Ala
NM_001311193.1:c.1363T>G NP_001298122.1:p.Ser455Ala
NM_024420.2:c.1543T>G NP_077734.1:p.Ser515Ala
XM_005245267.2:c.1432T>G XP_005245324.1:p.Ser478Ala
XM_011509641.1:c.1564T>G XP_011507943.1:p.Ser522Ala
XM_011509642.1:c.1543T>G XP_011507944.1:p.Ser515Ala
XM_011509643.1:c.1543T>G XP_011507945.1:p.Ser515Ala
XR_921838.1:n.1477+127T>G
XM_005245267.4:c.1558T>G XP_005245324.2:p.Ser520Ala
XM_011509642.2:c.1543T>G XP_011507944.1:p.Ser515Ala
NM_001311193.2:c.1363T>G NP_001298122.2:p.Ser455Ala
NM_024420.3:c.1543T>G MANE Select NP_077734.2:p.Ser515Ala