Canonical Allele Identifier: CA1302135315

Gene: PLA2R1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.160060986A= , CM000664.2:g.160060986A=	GRCh38
NC_000002.11:g.160917497A= , CM000664.1:g.160917497A=	GRCh37
NC_000002.10:g.160625743A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283243.13:c.109+1309T= MANE Select	ENSP00000283243.7:n.109+1309T=
ENST00000283243.11:c.109+1309T=	ENSP00000283243.7:n.109+1309T=
ENST00000392771.1:c.109+1309T=	ENSP00000376524.1:n.109+1309T=
NM_001007267.2:c.109+1309T=	NP_001007268.1:n.109+1309T=
NM_001195641.1:c.109+1309T=	NP_001182570.1:n.109+1309T=
NM_007366.4:c.109+1309T=	NP_031392.3:n.109+1309T=
XM_005246392.2:c.109+1309T=	XP_005246449.1:n.109+1309T=
XM_005246393.2:c.109+1309T=	XP_005246450.1:n.109+1309T=
XM_011510820.1:c.109+1309T=	XP_011509122.1:n.109+1309T=
XR_922892.1:n.608+1309T=
XR_923525.1:n.1038+33A=
XM_005246392.4:c.109+1309T=	XP_005246449.1:n.109+1309T=
XM_011510820.3:c.109+1309T=	XP_011509122.1:n.109+1309T=
XM_017003598.1:c.109+1309T=	XP_016859087.1:n.109+1309T=
XM_017003599.1:c.109+1309T=	XP_016859088.1:n.109+1309T=
XM_017003601.2:c.109+1309T=	XP_016859090.1:n.109+1309T=
XR_001738671.2:n.209+1309T=
XR_001738672.2:n.209+1309T=
XR_001738673.1:n.209+1309T=
XR_922892.3:n.209+1309T=
NM_007366.5:c.109+1309T= MANE Select	NP_031392.3:n.109+1309T=
NM_001195641.2:c.109+1309T=	NP_001182570.1:n.109+1309T=
NM_001007267.3:c.109+1309T=	NP_001007268.1:n.109+1309T=