Canonical Allele Identifier: CA33556605

Gene: PLA2G4A

Linked Data

• dbSNP Id: rs865940075
• MyVariant Identifiers: chr1:g.186925266C>T (hg19) ; chr1:g.186956134C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956134C>T , CM000663.2:g.186956134C>T	GRCh38
NC_000001.10:g.186925266C>T , CM000663.1:g.186925266C>T	GRCh37
NC_000001.9:g.185191889C>T	NCBI36
NG_012203.1:g.132235C>T
NG_012203.2:g.132235C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1369C>T MANE Select	ENSP00000356436.3:p.Gln457Ter
ENST00000367466.3:c.1369C>T	ENSP00000356436.3:p.Gln457Ter
NM_001311193.1:c.1189C>T	NP_001298122.1:p.Gln397Ter
NM_024420.2:c.1369C>T	NP_077734.1:p.Gln457Ter
XM_005245267.2:c.1258C>T	XP_005245324.1:p.Gln420Ter
XM_011509641.1:c.1390C>T	XP_011507943.1:p.Gln464Ter
XM_011509642.1:c.1369C>T	XP_011507944.1:p.Gln457Ter
XM_011509643.1:c.1369C>T	XP_011507945.1:p.Gln457Ter
XR_921838.1:n.1430C>T
XM_005245267.4:c.1384C>T	XP_005245324.2:p.Gln462Ter
XM_011509642.2:c.1369C>T	XP_011507944.1:p.Gln457Ter
NM_001311193.2:c.1189C>T	NP_001298122.2:p.Gln397Ter
NM_024420.3:c.1369C>T MANE Select	NP_077734.2:p.Gln457Ter