Canonical Allele Identifier: CA1465408635

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740093C= , CM000666.2:g.67740093C=	GRCh38
NC_000004.11:g.68605811C= , CM000666.1:g.68605811C=	GRCh37
NC_000004.10:g.68288406C=	NCBI36
NG_009293.1:g.20994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*387G= MANE Select	ENSP00000226413.5:n.*387G=
ENST00000226413.4:c.*387G=	ENSP00000226413.4:n.*387G=
NM_000406.2:c.*387G=	NP_000397.1:n.*387G=
NM_001012763.1:c.*496G=	NP_001012781.1:n.*496G=
NM_000406.3:c.*387G= MANE Select	NP_000397.1:n.*387G=
NM_001012763.2:c.*496G=	NP_001012781.1:n.*496G=