Canonical Allele Identifier: CA1465408703

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740134T= , CM000666.2:g.67740134T=	GRCh38
NC_000004.11:g.68605852T= , CM000666.1:g.68605852T=	GRCh37
NC_000004.10:g.68288447T=	NCBI36
NG_009293.1:g.20953A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*346A= MANE Select	ENSP00000226413.5:n.*346A=
ENST00000226413.4:c.*346A=	ENSP00000226413.4:n.*346A=
NM_000406.2:c.*346A=	NP_000397.1:n.*346A=
NM_001012763.1:c.*455A=	NP_001012781.1:n.*455A=
NM_000406.3:c.*346A= MANE Select	NP_000397.1:n.*346A=
NM_001012763.2:c.*455A=	NP_001012781.1:n.*455A=