Canonical Allele Identifier: CA1465409128

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740631C= , CM000666.2:g.67740631C=	GRCh38
NC_000004.11:g.68606349C= , CM000666.1:g.68606349C=	GRCh37
NC_000004.10:g.68288944C=	NCBI36
NG_009293.1:g.20456G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.836G= MANE Select	ENSP00000226413.5:p.Cys279=
ENST00000226413.4:c.836G=	ENSP00000226413.4:p.Cys279=
ENST00000420975.2:c.708G=	ENSP00000397561.2:p.Leu236=
NM_000406.2:c.836G=	NP_000397.1:p.Cys279=
NM_001012763.1:c.708G=	NP_001012781.1:p.Leu236=
NM_000406.3:c.836G= MANE Select	NP_000397.1:p.Cys279=
NM_001012763.2:c.708G=	NP_001012781.1:p.Leu236=