Canonical Allele Identifier: CA343952524

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925413C>T (hg19) ; chr1:g.186956281C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956281C>T , CM000663.2:g.186956281C>T	GRCh38
NC_000001.10:g.186925413C>T , CM000663.1:g.186925413C>T	GRCh37
NC_000001.9:g.185192036C>T	NCBI36
NG_012203.1:g.132382C>T
NG_012203.2:g.132382C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1516C>T MANE Select	ENSP00000356436.3:p.Pro506Ser
ENST00000367466.3:c.1516C>T	ENSP00000356436.3:p.Pro506Ser
NM_001311193.1:c.1336C>T	NP_001298122.1:p.Pro446Ser
NM_024420.2:c.1516C>T	NP_077734.1:p.Pro506Ser
XM_005245267.2:c.1405C>T	XP_005245324.1:p.Pro469Ser
XM_011509641.1:c.1537C>T	XP_011507943.1:p.Pro513Ser
XM_011509642.1:c.1516C>T	XP_011507944.1:p.Pro506Ser
XM_011509643.1:c.1516C>T	XP_011507945.1:p.Pro506Ser
XR_921838.1:n.1477+100C>T
XM_005245267.4:c.1531C>T	XP_005245324.2:p.Pro511Ser
XM_011509642.2:c.1516C>T	XP_011507944.1:p.Pro506Ser
NM_001311193.2:c.1336C>T	NP_001298122.2:p.Pro446Ser
NM_024420.3:c.1516C>T MANE Select	NP_077734.2:p.Pro506Ser