Canonical Allele Identifier: CA422343223

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925355T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956223T>A , CM000663.2:g.186956223T>A	GRCh38
NC_000001.10:g.186925355T>A , CM000663.1:g.186925355T>A	GRCh37
NC_000001.9:g.185191978T>A	NCBI36
NG_012203.1:g.132324T>A
NG_012203.2:g.132324T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1458T>A MANE Select	ENSP00000356436.3:p.Ala486=
ENST00000367466.3:c.1458T>A	ENSP00000356436.3:p.Ala486=
NM_001311193.1:c.1278T>A	NP_001298122.1:p.Ala426=
NM_024420.2:c.1458T>A	NP_077734.1:p.Ala486=
XM_005245267.2:c.1347T>A	XP_005245324.1:p.Ala449=
XM_011509641.1:c.1479T>A	XP_011507943.1:p.Ala493=
XM_011509642.1:c.1458T>A	XP_011507944.1:p.Ala486=
XM_011509643.1:c.1458T>A	XP_011507945.1:p.Ala486=
XR_921838.1:n.1477+42T>A
XM_005245267.4:c.1473T>A	XP_005245324.2:p.Ala491=
XM_011509642.2:c.1458T>A	XP_011507944.1:p.Ala486=
NM_001311193.2:c.1278T>A	NP_001298122.2:p.Ala426=
NM_024420.3:c.1458T>A MANE Select	NP_077734.2:p.Ala486=