Canonical Allele Identifier: CA1465409145

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740654T= , CM000666.2:g.67740654T=	GRCh38
NC_000004.11:g.68606372T= , CM000666.1:g.68606372T=	GRCh37
NC_000004.10:g.68288967T=	NCBI36
NG_009293.1:g.20433A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.813A= MANE Select	ENSP00000226413.5:p.Ala271=
ENST00000226413.4:c.813A=	ENSP00000226413.4:p.Ala271=
ENST00000420975.2:c.685A=	ENSP00000397561.2:p.Ile229=
NM_000406.2:c.813A=	NP_000397.1:p.Ala271=
NM_001012763.1:c.685A=	NP_001012781.1:p.Ile229=
NM_000406.3:c.813A= MANE Select	NP_000397.1:p.Ala271=
NM_001012763.2:c.685A=	NP_001012781.1:p.Ile229=