Canonical Allele Identifier: CA343952538

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925417T>A (hg19) ; chr1:g.186956285T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956285T>A , CM000663.2:g.186956285T>A	GRCh38
NC_000001.10:g.186925417T>A , CM000663.1:g.186925417T>A	GRCh37
NC_000001.9:g.185192040T>A	NCBI36
NG_012203.1:g.132386T>A
NG_012203.2:g.132386T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1520T>A MANE Select	ENSP00000356436.3:p.Leu507Ter
ENST00000367466.3:c.1520T>A	ENSP00000356436.3:p.Leu507Ter
NM_001311193.1:c.1340T>A	NP_001298122.1:p.Leu447Ter
NM_024420.2:c.1520T>A	NP_077734.1:p.Leu507Ter
XM_005245267.2:c.1409T>A	XP_005245324.1:p.Leu470Ter
XM_011509641.1:c.1541T>A	XP_011507943.1:p.Leu514Ter
XM_011509642.1:c.1520T>A	XP_011507944.1:p.Leu507Ter
XM_011509643.1:c.1520T>A	XP_011507945.1:p.Leu507Ter
XR_921838.1:n.1477+104T>A
XM_005245267.4:c.1535T>A	XP_005245324.2:p.Leu512Ter
XM_011509642.2:c.1520T>A	XP_011507944.1:p.Leu507Ter
NM_001311193.2:c.1340T>A	NP_001298122.2:p.Leu447Ter
NM_024420.3:c.1520T>A MANE Select	NP_077734.2:p.Leu507Ter