Canonical Allele Identifier: CA1143557118
Gene: PLA2G4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186956164C= , CM000663.2:g.186956164C= GRCh38
NC_000001.10:g.186925296C= , CM000663.1:g.186925296C= GRCh37
NC_000001.9:g.185191919C= NCBI36
NG_012203.1:g.132265C=
NG_012203.2:g.132265C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.1399C= MANE Select ENSP00000356436.3:p.Arg467=
ENST00000367466.3:c.1399C= ENSP00000356436.3:p.Arg467=
NM_001311193.1:c.1219C= NP_001298122.1:p.Arg407=
NM_024420.2:c.1399C= NP_077734.1:p.Arg467=
XM_005245267.2:c.1288C= XP_005245324.1:p.Arg430=
XM_011509641.1:c.1420C= XP_011507943.1:p.Arg474=
XM_011509642.1:c.1399C= XP_011507944.1:p.Arg467=
XM_011509643.1:c.1399C= XP_011507945.1:p.Arg467=
XR_921838.1:n.1460C=
XM_005245267.4:c.1414C= XP_005245324.2:p.Arg472=
XM_011509642.2:c.1399C= XP_011507944.1:p.Arg467=
NM_001311193.2:c.1219C= NP_001298122.2:p.Arg407=
NM_024420.3:c.1399C= MANE Select NP_077734.2:p.Arg467=