Canonical Allele Identifier: CA343952130

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs781508988
• gnomAD v4: 1-186956229-G-T
• MyVariant Identifiers: chr1:g.186925361G>T (hg19) ; chr1:g.186956229G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956229G>T , CM000663.2:g.186956229G>T	GRCh38
NC_000001.10:g.186925361G>T , CM000663.1:g.186925361G>T	GRCh37
NC_000001.9:g.185191984G>T	NCBI36
NG_012203.1:g.132330G>T
NG_012203.2:g.132330G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1464G>T MANE Select	ENSP00000356436.3:p.Lys488Asn
ENST00000367466.3:c.1464G>T	ENSP00000356436.3:p.Lys488Asn
NM_001311193.1:c.1284G>T	NP_001298122.1:p.Lys428Asn
NM_024420.2:c.1464G>T	NP_077734.1:p.Lys488Asn
XM_005245267.2:c.1353G>T	XP_005245324.1:p.Lys451Asn
XM_011509641.1:c.1485G>T	XP_011507943.1:p.Lys495Asn
XM_011509642.1:c.1464G>T	XP_011507944.1:p.Lys488Asn
XM_011509643.1:c.1464G>T	XP_011507945.1:p.Lys488Asn
XR_921838.1:n.1477+48G>T
XM_005245267.4:c.1479G>T	XP_005245324.2:p.Lys493Asn
XM_011509642.2:c.1464G>T	XP_011507944.1:p.Lys488Asn
NM_001311193.2:c.1284G>T	NP_001298122.2:p.Lys428Asn
NM_024420.3:c.1464G>T MANE Select	NP_077734.2:p.Lys488Asn