Canonical Allele Identifier: CA1465408718

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740153C= , CM000666.2:g.67740153C=	GRCh38
NC_000004.11:g.68605871C= , CM000666.1:g.68605871C=	GRCh37
NC_000004.10:g.68288466C=	NCBI36
NG_009293.1:g.20934G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*327G= MANE Select	ENSP00000226413.5:n.*327G=
ENST00000226413.4:c.*327G=	ENSP00000226413.4:n.*327G=
NM_000406.2:c.*327G=	NP_000397.1:n.*327G=
NM_001012763.1:c.*436G=	NP_001012781.1:n.*436G=
NM_000406.3:c.*327G= MANE Select	NP_000397.1:n.*327G=
NM_001012763.2:c.*436G=	NP_001012781.1:n.*436G=