Canonical Allele Identifier: CA2465564792

Gene: GPR50

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181303C= , CM000685.2:g.151181303C=	GRCh38
NC_000023.10:g.150349775C= , CM000685.1:g.150349775C=	GRCh37
NC_000023.9:g.150100433C=	NCBI36
NG_016405.1:g.9720C=
NG_016405.2:g.9720C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218316.4:c.1720C= MANE Select	ENSP00000218316.3:p.Pro574=
ENST00000218316.3:c.1720C=	ENSP00000218316.3:p.Pro574=
ENST00000617907.1:c.1714C=	ENSP00000484496.1:p.Pro572=
NM_004224.3:c.1720C= MANE Select	NP_004215.2:p.Pro574=
XM_011531216.1:c.979C=	XP_011529518.1:p.Pro327=
XM_011531216.2:c.979C=	XP_011529518.1:p.Pro327=