Canonical Allele Identifier: CA343952573

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs1656750802
• MyVariant Identifiers: chr1:g.186925424C>A (hg19) ; chr1:g.186956292C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956292C>A , CM000663.2:g.186956292C>A	GRCh38
NC_000001.10:g.186925424C>A , CM000663.1:g.186925424C>A	GRCh37
NC_000001.9:g.185192047C>A	NCBI36
NG_012203.1:g.132393C>A
NG_012203.2:g.132393C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1527C>A MANE Select	ENSP00000356436.3:p.Asp509Glu
ENST00000367466.3:c.1527C>A	ENSP00000356436.3:p.Asp509Glu
NM_001311193.1:c.1347C>A	NP_001298122.1:p.Asp449Glu
NM_024420.2:c.1527C>A	NP_077734.1:p.Asp509Glu
XM_005245267.2:c.1416C>A	XP_005245324.1:p.Asp472Glu
XM_011509641.1:c.1548C>A	XP_011507943.1:p.Asp516Glu
XM_011509642.1:c.1527C>A	XP_011507944.1:p.Asp509Glu
XM_011509643.1:c.1527C>A	XP_011507945.1:p.Asp509Glu
XR_921838.1:n.1477+111C>A
XM_005245267.4:c.1542C>A	XP_005245324.2:p.Asp514Glu
XM_011509642.2:c.1527C>A	XP_011507944.1:p.Asp509Glu
NM_001311193.2:c.1347C>A	NP_001298122.2:p.Asp449Glu
NM_024420.3:c.1527C>A MANE Select	NP_077734.2:p.Asp509Glu