Canonical Allele Identifier: CA1300220

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs578200626
• ExAC: 1:186925293 C / A
• gnomAD v2: 1-186925293-C-A
• gnomAD v3: 1-186956161-C-A
• gnomAD v4: 1-186956161-C-A
• MyVariant Identifiers: chr1:g.186925293C>A (hg19) ; chr1:g.186956161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956161C>A , CM000663.2:g.186956161C>A	GRCh38
NC_000001.10:g.186925293C>A , CM000663.1:g.186925293C>A	GRCh37
NC_000001.9:g.185191916C>A	NCBI36
NG_012203.1:g.132262C>A
NG_012203.2:g.132262C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1396C>A MANE Select	ENSP00000356436.3:p.His466Asn
ENST00000367466.3:c.1396C>A	ENSP00000356436.3:p.His466Asn
NM_001311193.1:c.1216C>A	NP_001298122.1:p.His406Asn
NM_024420.2:c.1396C>A	NP_077734.1:p.His466Asn
XM_005245267.2:c.1285C>A	XP_005245324.1:p.His429Asn
XM_011509641.1:c.1417C>A	XP_011507943.1:p.His473Asn
XM_011509642.1:c.1396C>A	XP_011507944.1:p.His466Asn
XM_011509643.1:c.1396C>A	XP_011507945.1:p.His466Asn
XR_921838.1:n.1457C>A
XM_005245267.4:c.1411C>A	XP_005245324.2:p.His471Asn
XM_011509642.2:c.1396C>A	XP_011507944.1:p.His466Asn
NM_001311193.2:c.1216C>A	NP_001298122.2:p.His406Asn
NM_024420.3:c.1396C>A MANE Select	NP_077734.2:p.His466Asn