Canonical Allele Identifier: CA343952389

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925390T>A (hg19) ; chr1:g.186956258T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956258T>A , CM000663.2:g.186956258T>A	GRCh38
NC_000001.10:g.186925390T>A , CM000663.1:g.186925390T>A	GRCh37
NC_000001.9:g.185192013T>A	NCBI36
NG_012203.1:g.132359T>A
NG_012203.2:g.132359T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1493T>A MANE Select	ENSP00000356436.3:p.Leu498His
ENST00000367466.3:c.1493T>A	ENSP00000356436.3:p.Leu498His
NM_001311193.1:c.1313T>A	NP_001298122.1:p.Leu438His
NM_024420.2:c.1493T>A	NP_077734.1:p.Leu498His
XM_005245267.2:c.1382T>A	XP_005245324.1:p.Leu461His
XM_011509641.1:c.1514T>A	XP_011507943.1:p.Leu505His
XM_011509642.1:c.1493T>A	XP_011507944.1:p.Leu498His
XM_011509643.1:c.1493T>A	XP_011507945.1:p.Leu498His
XR_921838.1:n.1477+77T>A
XM_005245267.4:c.1508T>A	XP_005245324.2:p.Leu503His
XM_011509642.2:c.1493T>A	XP_011507944.1:p.Leu498His
NM_001311193.2:c.1313T>A	NP_001298122.2:p.Leu438His
NM_024420.3:c.1493T>A MANE Select	NP_077734.2:p.Leu498His