Canonical Allele Identifier: CA1465408653

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740108C= , CM000666.2:g.67740108C=	GRCh38
NC_000004.11:g.68605826C= , CM000666.1:g.68605826C=	GRCh37
NC_000004.10:g.68288421C=	NCBI36
NG_009293.1:g.20979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*372G= MANE Select	ENSP00000226413.5:n.*372G=
ENST00000226413.4:c.*372G=	ENSP00000226413.4:n.*372G=
NM_000406.2:c.*372G=	NP_000397.1:n.*372G=
NM_001012763.1:c.*481G=	NP_001012781.1:n.*481G=
NM_000406.3:c.*372G= MANE Select	NP_000397.1:n.*372G=
NM_001012763.2:c.*481G=	NP_001012781.1:n.*481G=