Canonical Allele Identifier: CA1465408713

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740147T= , CM000666.2:g.67740147T=	GRCh38
NC_000004.11:g.68605865T= , CM000666.1:g.68605865T=	GRCh37
NC_000004.10:g.68288460T=	NCBI36
NG_009293.1:g.20940A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*333A= MANE Select	ENSP00000226413.5:n.*333A=
ENST00000226413.4:c.*333A=	ENSP00000226413.4:n.*333A=
NM_000406.2:c.*333A=	NP_000397.1:n.*333A=
NM_001012763.1:c.*442A=	NP_001012781.1:n.*442A=
NM_000406.3:c.*333A= MANE Select	NP_000397.1:n.*333A=
NM_001012763.2:c.*442A=	NP_001012781.1:n.*442A=