Canonical Allele Identifier: CA1465408641

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740095T= , CM000666.2:g.67740095T=	GRCh38
NC_000004.11:g.68605813T= , CM000666.1:g.68605813T=	GRCh37
NC_000004.10:g.68288408T=	NCBI36
NG_009293.1:g.20992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*385A= MANE Select	ENSP00000226413.5:n.*385A=
ENST00000226413.4:c.*385A=	ENSP00000226413.4:n.*385A=
NM_000406.2:c.*385A=	NP_000397.1:n.*385A=
NM_001012763.1:c.*494A=	NP_001012781.1:n.*494A=
NM_000406.3:c.*385A= MANE Select	NP_000397.1:n.*385A=
NM_001012763.2:c.*494A=	NP_001012781.1:n.*494A=