Canonical Allele Identifier: CA1465408681

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740122T= , CM000666.2:g.67740122T=	GRCh38
NC_000004.11:g.68605840T= , CM000666.1:g.68605840T=	GRCh37
NC_000004.10:g.68288435T=	NCBI36
NG_009293.1:g.20965A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*358A= MANE Select	ENSP00000226413.5:n.*358A=
ENST00000226413.4:c.*358A=	ENSP00000226413.4:n.*358A=
NM_000406.2:c.*358A=	NP_000397.1:n.*358A=
NM_001012763.1:c.*467A=	NP_001012781.1:n.*467A=
NM_000406.3:c.*358A= MANE Select	NP_000397.1:n.*358A=
NM_001012763.2:c.*467A=	NP_001012781.1:n.*467A=