Canonical Allele Identifier: CA422343221

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925352T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956220T>G , CM000663.2:g.186956220T>G	GRCh38
NC_000001.10:g.186925352T>G , CM000663.1:g.186925352T>G	GRCh37
NC_000001.9:g.185191975T>G	NCBI36
NG_012203.1:g.132321T>G
NG_012203.2:g.132321T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1455T>G MANE Select	ENSP00000356436.3:p.Arg485=
ENST00000367466.3:c.1455T>G	ENSP00000356436.3:p.Arg485=
NM_001311193.1:c.1275T>G	NP_001298122.1:p.Arg425=
NM_024420.2:c.1455T>G	NP_077734.1:p.Arg485=
XM_005245267.2:c.1344T>G	XP_005245324.1:p.Arg448=
XM_011509641.1:c.1476T>G	XP_011507943.1:p.Arg492=
XM_011509642.1:c.1455T>G	XP_011507944.1:p.Arg485=
XM_011509643.1:c.1455T>G	XP_011507945.1:p.Arg485=
XR_921838.1:n.1477+39T>G
XM_005245267.4:c.1470T>G	XP_005245324.2:p.Arg490=
XM_011509642.2:c.1455T>G	XP_011507944.1:p.Arg485=
NM_001311193.2:c.1275T>G	NP_001298122.2:p.Arg425=
NM_024420.3:c.1455T>G MANE Select	NP_077734.2:p.Arg485=