Canonical Allele Identifier: CA343951823

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925326G>T (hg19) ; chr1:g.186956194G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956194G>T , CM000663.2:g.186956194G>T	GRCh38
NC_000001.10:g.186925326G>T , CM000663.1:g.186925326G>T	GRCh37
NC_000001.9:g.185191949G>T	NCBI36
NG_012203.1:g.132295G>T
NG_012203.2:g.132295G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1429G>T MANE Select	ENSP00000356436.3:p.Ala477Ser
ENST00000367466.3:c.1429G>T	ENSP00000356436.3:p.Ala477Ser
NM_001311193.1:c.1249G>T	NP_001298122.1:p.Ala417Ser
NM_024420.2:c.1429G>T	NP_077734.1:p.Ala477Ser
XM_005245267.2:c.1318G>T	XP_005245324.1:p.Ala440Ser
XM_011509641.1:c.1450G>T	XP_011507943.1:p.Ala484Ser
XM_011509642.1:c.1429G>T	XP_011507944.1:p.Ala477Ser
XM_011509643.1:c.1429G>T	XP_011507945.1:p.Ala477Ser
XR_921838.1:n.1477+13G>T
XM_005245267.4:c.1444G>T	XP_005245324.2:p.Ala482Ser
XM_011509642.2:c.1429G>T	XP_011507944.1:p.Ala477Ser
NM_001311193.2:c.1249G>T	NP_001298122.2:p.Ala417Ser
NM_024420.3:c.1429G>T MANE Select	NP_077734.2:p.Ala477Ser