Canonical Allele Identifier: CA1465409099

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740610A= , CM000666.2:g.67740610A=	GRCh38
NC_000004.11:g.68606328A= , CM000666.1:g.68606328A=	GRCh37
NC_000004.10:g.68288923A=	NCBI36
NG_009293.1:g.20477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.857T= MANE Select	ENSP00000226413.5:p.Leu286=
ENST00000226413.4:c.857T=	ENSP00000226413.4:p.Leu286=
ENST00000420975.2:c.729T=	ENSP00000397561.2:p.Pro243=
NM_000406.2:c.857T=	NP_000397.1:p.Leu286=
NM_001012763.1:c.729T=	NP_001012781.1:p.Pro243=
NM_000406.3:c.857T= MANE Select	NP_000397.1:p.Leu286=
NM_001012763.2:c.729T=	NP_001012781.1:p.Pro243=