Canonical Allele Identifier: CA343951980

Gene: PLA2G4A

Linked Data

• COSMIC: COSM424849
• MyVariant Identifiers: chr1:g.186925342G>C (hg19) ; chr1:g.186956210G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956210G>C , CM000663.2:g.186956210G>C	GRCh38
NC_000001.10:g.186925342G>C , CM000663.1:g.186925342G>C	GRCh37
NC_000001.9:g.185191965G>C	NCBI36
NG_012203.1:g.132311G>C
NG_012203.2:g.132311G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1445G>C MANE Select	ENSP00000356436.3:p.Arg482Thr
ENST00000367466.3:c.1445G>C	ENSP00000356436.3:p.Arg482Thr
NM_001311193.1:c.1265G>C	NP_001298122.1:p.Arg422Thr
NM_024420.2:c.1445G>C	NP_077734.1:p.Arg482Thr
XM_005245267.2:c.1334G>C	XP_005245324.1:p.Arg445Thr
XM_011509641.1:c.1466G>C	XP_011507943.1:p.Arg489Thr
XM_011509642.1:c.1445G>C	XP_011507944.1:p.Arg482Thr
XM_011509643.1:c.1445G>C	XP_011507945.1:p.Arg482Thr
XR_921838.1:n.1477+29G>C
XM_005245267.4:c.1460G>C	XP_005245324.2:p.Arg487Thr
XM_011509642.2:c.1445G>C	XP_011507944.1:p.Arg482Thr
NM_001311193.2:c.1265G>C	NP_001298122.2:p.Arg422Thr
NM_024420.3:c.1445G>C MANE Select	NP_077734.2:p.Arg482Thr