Canonical Allele Identifier: CA2465564813

Gene: GPR50

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181350_151181357delinsCCCTACTG , CM000685.2:g.151181350_151181357delinsCCCTACTG	GRCh38
NC_000023.10:g.150349822_150349829delinsCCCTACTG , CM000685.1:g.150349822_150349829delinsCCCTACTG	GRCh37
NC_000023.9:g.150100480_150100487delinsCCCTACTG	NCBI36
NG_016405.1:g.9767_9774delinsCCCTACTG
NG_016405.2:g.9767_9774delinsCCCTACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1767_1774delinsCCCTACTG MANE Select	ENSP00000218316.3:p.Asp589=
ENST00000218316.3:c.1767_1774delinsCCCTACTG	ENSP00000218316.3:p.Asp589=
ENST00000617907.1:c.1761_1768delinsCCCTACTG	ENSP00000484496.1:p.Asp587=
NM_004224.3:c.1767_1774delinsCCCTACTG MANE Select	NP_004215.2:p.Asp589=
XM_011531216.1:c.1026_1033delinsCCCTACTG	XP_011529518.1:p.Asp342=
XM_011531216.2:c.1026_1033delinsCCCTACTG	XP_011529518.1:p.Asp342=