Canonical Allele Identifier: CA1213368222
Gene: PLA2G4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186956167A= , CM000663.2:g.186956167A= GRCh38
NC_000001.10:g.186925299A= , CM000663.1:g.186925299A= GRCh37
NC_000001.9:g.185191922A= NCBI36
NG_012203.1:g.132268A=
NG_012203.2:g.132268A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.1402A= MANE Select ENSP00000356436.3:p.Met468=
ENST00000367466.3:c.1402A= ENSP00000356436.3:p.Met468=
NM_001311193.1:c.1222A= NP_001298122.1:p.Met408=
NM_024420.2:c.1402A= NP_077734.1:p.Met468=
XM_005245267.2:c.1291A= XP_005245324.1:p.Met431=
XM_011509641.1:c.1423A= XP_011507943.1:p.Met475=
XM_011509642.1:c.1402A= XP_011507944.1:p.Met468=
XM_011509643.1:c.1402A= XP_011507945.1:p.Met468=
XR_921838.1:n.1463A=
XM_005245267.4:c.1417A= XP_005245324.2:p.Met473=
XM_011509642.2:c.1402A= XP_011507944.1:p.Met468=
NM_001311193.2:c.1222A= NP_001298122.2:p.Met408=
NM_024420.3:c.1402A= MANE Select NP_077734.2:p.Met468=