Canonical Allele Identifier: CA343951540

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925285G>T (hg19) ; chr1:g.186956153G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956153G>T , CM000663.2:g.186956153G>T	GRCh38
NC_000001.10:g.186925285G>T , CM000663.1:g.186925285G>T	GRCh37
NC_000001.9:g.185191908G>T	NCBI36
NG_012203.1:g.132254G>T
NG_012203.2:g.132254G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1388G>T MANE Select	ENSP00000356436.3:p.Ser463Ile
ENST00000367466.3:c.1388G>T	ENSP00000356436.3:p.Ser463Ile
NM_001311193.1:c.1208G>T	NP_001298122.1:p.Ser403Ile
NM_024420.2:c.1388G>T	NP_077734.1:p.Ser463Ile
XM_005245267.2:c.1277G>T	XP_005245324.1:p.Ser426Ile
XM_011509641.1:c.1409G>T	XP_011507943.1:p.Ser470Ile
XM_011509642.1:c.1388G>T	XP_011507944.1:p.Ser463Ile
XM_011509643.1:c.1388G>T	XP_011507945.1:p.Ser463Ile
XR_921838.1:n.1449G>T
XM_005245267.4:c.1403G>T	XP_005245324.2:p.Ser468Ile
XM_011509642.2:c.1388G>T	XP_011507944.1:p.Ser463Ile
NM_001311193.2:c.1208G>T	NP_001298122.2:p.Ser403Ile
NM_024420.3:c.1388G>T MANE Select	NP_077734.2:p.Ser463Ile