Canonical Allele Identifier: CA1465408690

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740131T= , CM000666.2:g.67740131T=	GRCh38
NC_000004.11:g.68605849T= , CM000666.1:g.68605849T=	GRCh37
NC_000004.10:g.68288444T=	NCBI36
NG_009293.1:g.20956A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*349A= MANE Select	ENSP00000226413.5:n.*349A=
ENST00000226413.4:c.*349A=	ENSP00000226413.4:n.*349A=
NM_000406.2:c.*349A=	NP_000397.1:n.*349A=
NM_001012763.1:c.*458A=	NP_001012781.1:n.*458A=
NM_000406.3:c.*349A= MANE Select	NP_000397.1:n.*349A=
NM_001012763.2:c.*458A=	NP_001012781.1:n.*458A=