Canonical Allele Identifier: CA343951663

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925303T>G (hg19) ; chr1:g.186956171T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956171T>G , CM000663.2:g.186956171T>G	GRCh38
NC_000001.10:g.186925303T>G , CM000663.1:g.186925303T>G	GRCh37
NC_000001.9:g.185191926T>G	NCBI36
NG_012203.1:g.132272T>G
NG_012203.2:g.132272T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1406T>G MANE Select	ENSP00000356436.3:p.Ile469Arg
ENST00000367466.3:c.1406T>G	ENSP00000356436.3:p.Ile469Arg
NM_001311193.1:c.1226T>G	NP_001298122.1:p.Ile409Arg
NM_024420.2:c.1406T>G	NP_077734.1:p.Ile469Arg
XM_005245267.2:c.1295T>G	XP_005245324.1:p.Ile432Arg
XM_011509641.1:c.1427T>G	XP_011507943.1:p.Ile476Arg
XM_011509642.1:c.1406T>G	XP_011507944.1:p.Ile469Arg
XM_011509643.1:c.1406T>G	XP_011507945.1:p.Ile469Arg
XR_921838.1:n.1467T>G
XM_005245267.4:c.1421T>G	XP_005245324.2:p.Ile474Arg
XM_011509642.2:c.1406T>G	XP_011507944.1:p.Ile469Arg
NM_001311193.2:c.1226T>G	NP_001298122.2:p.Ile409Arg
NM_024420.3:c.1406T>G MANE Select	NP_077734.2:p.Ile469Arg