Canonical Allele Identifier: CA1142127328
Gene: PLA2G4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186956202C= , CM000663.2:g.186956202C= GRCh38
NC_000001.10:g.186925334C= , CM000663.1:g.186925334C= GRCh37
NC_000001.9:g.185191957C= NCBI36
NG_012203.1:g.132303C=
NG_012203.2:g.132303C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.1437C= MANE Select ENSP00000356436.3:p.Phe479=
ENST00000367466.3:c.1437C= ENSP00000356436.3:p.Phe479=
NM_001311193.1:c.1257C= NP_001298122.1:p.Phe419=
NM_024420.2:c.1437C= NP_077734.1:p.Phe479=
XM_005245267.2:c.1326C= XP_005245324.1:p.Phe442=
XM_011509641.1:c.1458C= XP_011507943.1:p.Phe486=
XM_011509642.1:c.1437C= XP_011507944.1:p.Phe479=
XM_011509643.1:c.1437C= XP_011507945.1:p.Phe479=
XR_921838.1:n.1477+21C=
XM_005245267.4:c.1452C= XP_005245324.2:p.Phe484=
XM_011509642.2:c.1437C= XP_011507944.1:p.Phe479=
NM_001311193.2:c.1257C= NP_001298122.2:p.Phe419=
NM_024420.3:c.1437C= MANE Select NP_077734.2:p.Phe479=