Canonical Allele Identifier: CA1465421023

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754342C= , CM000666.2:g.67754342C=	GRCh38
NC_000004.11:g.68620060C= , CM000666.1:g.68620060C=	GRCh37
NC_000004.10:g.68302655C=	NCBI36
NG_009293.1:g.6745G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.-7G= MANE Select	ENSP00000226413.5:n.-7G=
ENST00000226413.4:c.-7G=	ENSP00000226413.4:n.-7G=
NM_000406.2:c.-7G=	NP_000397.1:n.-7G=
NM_001012763.1:c.-7G=	NP_001012781.1:n.-7G=
NM_000406.3:c.-7G= MANE Select	NP_000397.1:n.-7G=
NM_001012763.2:c.-7G=	NP_001012781.1:n.-7G=