Canonical Allele Identifier: CA422343232

Gene: PLA2G4A

Linked Data

• COSMIC: COSM2123424
• MyVariant Identifiers: chr1:g.186925373C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956241C>T , CM000663.2:g.186956241C>T	GRCh38
NC_000001.10:g.186925373C>T , CM000663.1:g.186925373C>T	GRCh37
NC_000001.9:g.185191996C>T	NCBI36
NG_012203.1:g.132342C>T
NG_012203.2:g.132342C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1476C>T MANE Select	ENSP00000356436.3:p.Phe492=
ENST00000367466.3:c.1476C>T	ENSP00000356436.3:p.Phe492=
NM_001311193.1:c.1296C>T	NP_001298122.1:p.Phe432=
NM_024420.2:c.1476C>T	NP_077734.1:p.Phe492=
XM_005245267.2:c.1365C>T	XP_005245324.1:p.Phe455=
XM_011509641.1:c.1497C>T	XP_011507943.1:p.Phe499=
XM_011509642.1:c.1476C>T	XP_011507944.1:p.Phe492=
XM_011509643.1:c.1476C>T	XP_011507945.1:p.Phe492=
XR_921838.1:n.1477+60C>T
XM_005245267.4:c.1491C>T	XP_005245324.2:p.Phe497=
XM_011509642.2:c.1476C>T	XP_011507944.1:p.Phe492=
NM_001311193.2:c.1296C>T	NP_001298122.2:p.Phe432=
NM_024420.3:c.1476C>T MANE Select	NP_077734.2:p.Phe492=