Canonical Allele Identifier: CA422343226

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925358G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956226G>T , CM000663.2:g.186956226G>T	GRCh38
NC_000001.10:g.186925358G>T , CM000663.1:g.186925358G>T	GRCh37
NC_000001.9:g.185191981G>T	NCBI36
NG_012203.1:g.132327G>T
NG_012203.2:g.132327G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1461G>T MANE Select	ENSP00000356436.3:p.Gly487=
ENST00000367466.3:c.1461G>T	ENSP00000356436.3:p.Gly487=
NM_001311193.1:c.1281G>T	NP_001298122.1:p.Gly427=
NM_024420.2:c.1461G>T	NP_077734.1:p.Gly487=
XM_005245267.2:c.1350G>T	XP_005245324.1:p.Gly450=
XM_011509641.1:c.1482G>T	XP_011507943.1:p.Gly494=
XM_011509642.1:c.1461G>T	XP_011507944.1:p.Gly487=
XM_011509643.1:c.1461G>T	XP_011507945.1:p.Gly487=
XR_921838.1:n.1477+45G>T
XM_005245267.4:c.1476G>T	XP_005245324.2:p.Gly492=
XM_011509642.2:c.1461G>T	XP_011507944.1:p.Gly487=
NM_001311193.2:c.1281G>T	NP_001298122.2:p.Gly427=
NM_024420.3:c.1461G>T MANE Select	NP_077734.2:p.Gly487=