Canonical Allele Identifier: CA1300231

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs758124009
• ExAC: 1:186925331 A / G
• gnomAD v2: 1-186925331-A-G
• gnomAD v4: 1-186956199-A-G
• MyVariant Identifiers: chr1:g.186925331A>G (hg19) ; chr1:g.186956199A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956199A>G , CM000663.2:g.186956199A>G	GRCh38
NC_000001.10:g.186925331A>G , CM000663.1:g.186925331A>G	GRCh37
NC_000001.9:g.185191954A>G	NCBI36
NG_012203.1:g.132300A>G
NG_012203.2:g.132300A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1434A>G MANE Select	ENSP00000356436.3:p.Leu478=
ENST00000367466.3:c.1434A>G	ENSP00000356436.3:p.Leu478=
NM_001311193.1:c.1254A>G	NP_001298122.1:p.Leu418=
NM_024420.2:c.1434A>G	NP_077734.1:p.Leu478=
XM_005245267.2:c.1323A>G	XP_005245324.1:p.Leu441=
XM_011509641.1:c.1455A>G	XP_011507943.1:p.Leu485=
XM_011509642.1:c.1434A>G	XP_011507944.1:p.Leu478=
XM_011509643.1:c.1434A>G	XP_011507945.1:p.Leu478=
XR_921838.1:n.1477+18A>G
XM_005245267.4:c.1449A>G	XP_005245324.2:p.Leu483=
XM_011509642.2:c.1434A>G	XP_011507944.1:p.Leu478=
NM_001311193.2:c.1254A>G	NP_001298122.2:p.Leu418=
NM_024420.3:c.1434A>G MANE Select	NP_077734.2:p.Leu478=