Canonical Allele Identifier: CA1465409063

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740562T= , CM000666.2:g.67740562T=	GRCh38
NC_000004.11:g.68606280T= , CM000666.1:g.68606280T=	GRCh37
NC_000004.10:g.68288875T=	NCBI36
NG_009293.1:g.20525A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.905A= MANE Select	ENSP00000226413.5:p.Asp302=
ENST00000226413.4:c.905A=	ENSP00000226413.4:p.Asp302=
ENST00000420975.2:c.777A=	ENSP00000397561.2:n.777A=
NM_000406.2:c.905A=	NP_000397.1:p.Asp302=
NM_001012763.1:c.*27A=	NP_001012781.1:n.*27A=
NM_000406.3:c.905A= MANE Select	NP_000397.1:p.Asp302=
NM_001012763.2:c.*27A=	NP_001012781.1:n.*27A=