Canonical Allele Identifier: CA2517776391

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740215_67740216insACAA , CM000666.2:g.67740215_67740216insACAA	GRCh38
NC_000004.11:g.68605933_68605934insACAA , CM000666.1:g.68605933_68605934insACAA	GRCh37
NC_000004.10:g.68288528_68288529insACAA	NCBI36
NG_009293.1:g.20871_20872insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*264_*265insTTGT MANE Select	ENSP00000226413.5:n.*264_*265insTTGT
ENST00000226413.4:c.*264_*265insTTGT	ENSP00000226413.4:n.*264_*265insTTGT
NM_000406.2:c.*264_*265insTTGT	NP_000397.1:n.*264_*265insTTGT
NM_001012763.1:c.*373_*374insTTGT	NP_001012781.1:n.*373_*374insTTGT
NM_000406.3:c.*264_*265insTTGT MANE Select	NP_000397.1:n.*264_*265insTTGT
NM_001012763.2:c.*373_*374insTTGT	NP_001012781.1:n.*373_*374insTTGT