Canonical Allele Identifier: CA343952454

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs1400556637
• gnomAD v2: 1-186925402-A-C
• gnomAD v4: 1-186956270-A-C
• MyVariant Identifiers: chr1:g.186925402A>C (hg19) ; chr1:g.186956270A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956270A>C , CM000663.2:g.186956270A>C	GRCh38
NC_000001.10:g.186925402A>C , CM000663.1:g.186925402A>C	GRCh37
NC_000001.9:g.185192025A>C	NCBI36
NG_012203.1:g.132371A>C
NG_012203.2:g.132371A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1505A>C MANE Select	ENSP00000356436.3:p.Tyr502Ser
ENST00000367466.3:c.1505A>C	ENSP00000356436.3:p.Tyr502Ser
NM_001311193.1:c.1325A>C	NP_001298122.1:p.Tyr442Ser
NM_024420.2:c.1505A>C	NP_077734.1:p.Tyr502Ser
XM_005245267.2:c.1394A>C	XP_005245324.1:p.Tyr465Ser
XM_011509641.1:c.1526A>C	XP_011507943.1:p.Tyr509Ser
XM_011509642.1:c.1505A>C	XP_011507944.1:p.Tyr502Ser
XM_011509643.1:c.1505A>C	XP_011507945.1:p.Tyr502Ser
XR_921838.1:n.1477+89A>C
XM_005245267.4:c.1520A>C	XP_005245324.2:p.Tyr507Ser
XM_011509642.2:c.1505A>C	XP_011507944.1:p.Tyr502Ser
NM_001311193.2:c.1325A>C	NP_001298122.2:p.Tyr442Ser
NM_024420.3:c.1505A>C MANE Select	NP_077734.2:p.Tyr502Ser