Canonical Allele Identifier: CA1334541386

Gene: GPR55

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.230910379C= , CM000664.2:g.230910379C=	GRCh38
NC_000002.11:g.231775094C= , CM000664.1:g.231775094C=	GRCh37
NC_000002.10:g.231483338C=	NCBI36
NG_050956.1:g.55849G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650999.1:c.584G= MANE Select	ENSP00000498258.1:p.Gly195=
ENST00000392039.2:c.584G=	ENSP00000375893.2:p.Gly195=
ENST00000392040.5:c.584G=	ENSP00000375894.1:p.Gly195=
ENST00000438398.1:c.584G=	ENSP00000412768.1:p.Gly195=
ENST00000444078.5:c.584G=	ENSP00000410267.1:p.Gly195=
ENST00000622008.4:c.584G=	ENSP00000482381.1:p.Gly195=
NM_005683.3:c.584G=	NP_005674.2:p.Gly195=
XM_005246952.2:c.584G=	XP_005247009.1:p.Gly195=
XM_011512175.1:c.584G=	XP_011510477.1:p.Gly195=
XM_011512176.1:c.584G=	XP_011510478.1:p.Gly195=
XM_011512177.1:c.584G=	XP_011510479.1:p.Gly195=
XM_005246952.4:c.584G=	XP_005247009.1:p.Gly195=
XM_011512175.3:c.584G=	XP_011510477.1:p.Gly195=
XM_011512176.2:c.584G=	XP_011510478.1:p.Gly195=
NM_005683.4:c.584G= MANE Select	NP_005674.2:p.Gly195=