Canonical Allele Identifier: CA2465564835

Gene: GPR50

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181402G= , CM000685.2:g.151181402G=	GRCh38
NC_000023.10:g.150349874G= , CM000685.1:g.150349874G=	GRCh37
NC_000023.9:g.150100532G=	NCBI36
NG_016405.1:g.9819G=
NG_016405.2:g.9819G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1819G= MANE Select	ENSP00000218316.3:p.Asp607=
ENST00000218316.3:c.1819G=	ENSP00000218316.3:p.Asp607=
ENST00000617907.1:c.1813G=	ENSP00000484496.1:p.Asp605=
NM_004224.3:c.1819G= MANE Select	NP_004215.2:p.Asp607=
XM_011531216.1:c.1078G=	XP_011529518.1:p.Asp360=
XM_011531216.2:c.1078G=	XP_011529518.1:p.Asp360=