Canonical Allele Identifier: CA343951380

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925270G>A (hg19) ; chr1:g.186956138G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956138G>A , CM000663.2:g.186956138G>A	GRCh38
NC_000001.10:g.186925270G>A , CM000663.1:g.186925270G>A	GRCh37
NC_000001.9:g.185191893G>A	NCBI36
NG_012203.1:g.132239G>A
NG_012203.2:g.132239G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1373G>A MANE Select	ENSP00000356436.3:p.Ser458Asn
ENST00000367466.3:c.1373G>A	ENSP00000356436.3:p.Ser458Asn
NM_001311193.1:c.1193G>A	NP_001298122.1:p.Ser398Asn
NM_024420.2:c.1373G>A	NP_077734.1:p.Ser458Asn
XM_005245267.2:c.1262G>A	XP_005245324.1:p.Ser421Asn
XM_011509641.1:c.1394G>A	XP_011507943.1:p.Ser465Asn
XM_011509642.1:c.1373G>A	XP_011507944.1:p.Ser458Asn
XM_011509643.1:c.1373G>A	XP_011507945.1:p.Ser458Asn
XR_921838.1:n.1434G>A
XM_005245267.4:c.1388G>A	XP_005245324.2:p.Ser463Asn
XM_011509642.2:c.1373G>A	XP_011507944.1:p.Ser458Asn
NM_001311193.2:c.1193G>A	NP_001298122.2:p.Ser398Asn
NM_024420.3:c.1373G>A MANE Select	NP_077734.2:p.Ser458Asn