Canonical Allele Identifier: CA1144009670
Gene: PLA2G4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186956139T= , CM000663.2:g.186956139T= GRCh38
NC_000001.10:g.186925271T= , CM000663.1:g.186925271T= GRCh37
NC_000001.9:g.185191894T= NCBI36
NG_012203.1:g.132240T=
NG_012203.2:g.132240T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.1374T= MANE Select ENSP00000356436.3:p.Ser458=
ENST00000367466.3:c.1374T= ENSP00000356436.3:p.Ser458=
NM_001311193.1:c.1194T= NP_001298122.1:p.Ser398=
NM_024420.2:c.1374T= NP_077734.1:p.Ser458=
XM_005245267.2:c.1263T= XP_005245324.1:p.Ser421=
XM_011509641.1:c.1395T= XP_011507943.1:p.Ser465=
XM_011509642.1:c.1374T= XP_011507944.1:p.Ser458=
XM_011509643.1:c.1374T= XP_011507945.1:p.Ser458=
XR_921838.1:n.1435T=
XM_005245267.4:c.1389T= XP_005245324.2:p.Ser463=
XM_011509642.2:c.1374T= XP_011507944.1:p.Ser458=
NM_001311193.2:c.1194T= NP_001298122.2:p.Ser398=
NM_024420.3:c.1374T= MANE Select NP_077734.2:p.Ser458=