Canonical Allele Identifier: CA343951973

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925341A>T (hg19) ; chr1:g.186956209A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956209A>T , CM000663.2:g.186956209A>T	GRCh38
NC_000001.10:g.186925341A>T , CM000663.1:g.186925341A>T	GRCh37
NC_000001.9:g.185191964A>T	NCBI36
NG_012203.1:g.132310A>T
NG_012203.2:g.132310A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1444A>T MANE Select	ENSP00000356436.3:p.Arg482Ter
ENST00000367466.3:c.1444A>T	ENSP00000356436.3:p.Arg482Ter
NM_001311193.1:c.1264A>T	NP_001298122.1:p.Arg422Ter
NM_024420.2:c.1444A>T	NP_077734.1:p.Arg482Ter
XM_005245267.2:c.1333A>T	XP_005245324.1:p.Arg445Ter
XM_011509641.1:c.1465A>T	XP_011507943.1:p.Arg489Ter
XM_011509642.1:c.1444A>T	XP_011507944.1:p.Arg482Ter
XM_011509643.1:c.1444A>T	XP_011507945.1:p.Arg482Ter
XR_921838.1:n.1477+28A>T
XM_005245267.4:c.1459A>T	XP_005245324.2:p.Arg487Ter
XM_011509642.2:c.1444A>T	XP_011507944.1:p.Arg482Ter
NM_001311193.2:c.1264A>T	NP_001298122.2:p.Arg422Ter
NM_024420.3:c.1444A>T MANE Select	NP_077734.2:p.Arg482Ter