Canonical Allele Identifier: CA2465564802

Gene: GPR50

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181332C= , CM000685.2:g.151181332C=	GRCh38
NC_000023.10:g.150349804C= , CM000685.1:g.150349804C=	GRCh37
NC_000023.9:g.150100462C=	NCBI36
NG_016405.1:g.9749C=
NG_016405.2:g.9749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1749C= MANE Select	ENSP00000218316.3:p.Thr583=
ENST00000218316.3:c.1749C=	ENSP00000218316.3:p.Thr583=
ENST00000617907.1:c.1743C=	ENSP00000484496.1:p.Thr581=
NM_004224.3:c.1749C= MANE Select	NP_004215.2:p.Thr583=
XM_011531216.1:c.1008C=	XP_011529518.1:p.Thr336=
XM_011531216.2:c.1008C=	XP_011529518.1:p.Thr336=