Canonical Allele Identifier: CA343951739

Gene: PLA2G4A

Linked Data

• gnomAD v4: 1-186956182-G-A
• MyVariant Identifiers: chr1:g.186925314G>A (hg19) ; chr1:g.186956182G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956182G>A , CM000663.2:g.186956182G>A	GRCh38
NC_000001.10:g.186925314G>A , CM000663.1:g.186925314G>A	GRCh37
NC_000001.9:g.185191937G>A	NCBI36
NG_012203.1:g.132283G>A
NG_012203.2:g.132283G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1417G>A MANE Select	ENSP00000356436.3:p.Val473Met
ENST00000367466.3:c.1417G>A	ENSP00000356436.3:p.Val473Met
NM_001311193.1:c.1237G>A	NP_001298122.1:p.Val413Met
NM_024420.2:c.1417G>A	NP_077734.1:p.Val473Met
XM_005245267.2:c.1306G>A	XP_005245324.1:p.Val436Met
XM_011509641.1:c.1438G>A	XP_011507943.1:p.Val480Met
XM_011509642.1:c.1417G>A	XP_011507944.1:p.Val473Met
XM_011509643.1:c.1417G>A	XP_011507945.1:p.Val473Met
XR_921838.1:n.1477+1G>A
XM_005245267.4:c.1432G>A	XP_005245324.2:p.Val478Met
XM_011509642.2:c.1417G>A	XP_011507944.1:p.Val473Met
NM_001311193.2:c.1237G>A	NP_001298122.2:p.Val413Met
NM_024420.3:c.1417G>A MANE Select	NP_077734.2:p.Val473Met