Canonical Allele Identifier: CA422343270

Gene: PLA2G4A

Linked Data

• gnomAD v4: 1-186956298-C-T
• MyVariant Identifiers: chr1:g.186925430C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956298C>T , CM000663.2:g.186956298C>T	GRCh38
NC_000001.10:g.186925430C>T , CM000663.1:g.186925430C>T	GRCh37
NC_000001.9:g.185192053C>T	NCBI36
NG_012203.1:g.132399C>T
NG_012203.2:g.132399C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1533C>T MANE Select	ENSP00000356436.3:p.Ala511=
ENST00000367466.3:c.1533C>T	ENSP00000356436.3:p.Ala511=
NM_001311193.1:c.1353C>T	NP_001298122.1:p.Ala451=
NM_024420.2:c.1533C>T	NP_077734.1:p.Ala511=
XM_005245267.2:c.1422C>T	XP_005245324.1:p.Ala474=
XM_011509641.1:c.1554C>T	XP_011507943.1:p.Ala518=
XM_011509642.1:c.1533C>T	XP_011507944.1:p.Ala511=
XM_011509643.1:c.1533C>T	XP_011507945.1:p.Ala511=
XR_921838.1:n.1477+117C>T
XM_005245267.4:c.1548C>T	XP_005245324.2:p.Ala516=
XM_011509642.2:c.1533C>T	XP_011507944.1:p.Ala511=
NM_001311193.2:c.1353C>T	NP_001298122.2:p.Ala451=
NM_024420.3:c.1533C>T MANE Select	NP_077734.2:p.Ala511=