Canonical Allele Identifier: CA1465408687

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740128C= , CM000666.2:g.67740128C=	GRCh38
NC_000004.11:g.68605846C= , CM000666.1:g.68605846C=	GRCh37
NC_000004.10:g.68288441C=	NCBI36
NG_009293.1:g.20959G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*352G= MANE Select	ENSP00000226413.5:n.*352G=
ENST00000226413.4:c.*352G=	ENSP00000226413.4:n.*352G=
NM_000406.2:c.*352G=	NP_000397.1:n.*352G=
NM_001012763.1:c.*461G=	NP_001012781.1:n.*461G=
NM_000406.3:c.*352G= MANE Select	NP_000397.1:n.*352G=
NM_001012763.2:c.*461G=	NP_001012781.1:n.*461G=