Canonical Allele Identifier: CA422343227

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925364A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956232A>C , CM000663.2:g.186956232A>C	GRCh38
NC_000001.10:g.186925364A>C , CM000663.1:g.186925364A>C	GRCh37
NC_000001.9:g.185191987A>C	NCBI36
NG_012203.1:g.132333A>C
NG_012203.2:g.132333A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1467A>C MANE Select	ENSP00000356436.3:p.Val489=
ENST00000367466.3:c.1467A>C	ENSP00000356436.3:p.Val489=
NM_001311193.1:c.1287A>C	NP_001298122.1:p.Val429=
NM_024420.2:c.1467A>C	NP_077734.1:p.Val489=
XM_005245267.2:c.1356A>C	XP_005245324.1:p.Val452=
XM_011509641.1:c.1488A>C	XP_011507943.1:p.Val496=
XM_011509642.1:c.1467A>C	XP_011507944.1:p.Val489=
XM_011509643.1:c.1467A>C	XP_011507945.1:p.Val489=
XR_921838.1:n.1477+51A>C
XM_005245267.4:c.1482A>C	XP_005245324.2:p.Val494=
XM_011509642.2:c.1467A>C	XP_011507944.1:p.Val489=
NM_001311193.2:c.1287A>C	NP_001298122.2:p.Val429=
NM_024420.3:c.1467A>C MANE Select	NP_077734.2:p.Val489=