Canonical Allele Identifier: CA1465420343

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753736T= , CM000666.2:g.67753736T=	GRCh38
NC_000004.11:g.68619454T= , CM000666.1:g.68619454T=	GRCh37
NC_000004.10:g.68302049T=	NCBI36
NG_009293.1:g.7351A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.522+78A= MANE Select	ENSP00000226413.5:n.522+78A=
ENST00000226413.4:c.522+78A=	ENSP00000226413.4:n.522+78A=
ENST00000420975.2:c.522+78A=	ENSP00000397561.2:n.522+78A=
NM_000406.2:c.522+78A=	NP_000397.1:n.522+78A=
NM_001012763.1:c.522+78A=	NP_001012781.1:n.522+78A=
NM_000406.3:c.522+78A= MANE Select	NP_000397.1:n.522+78A=
NM_001012763.2:c.522+78A=	NP_001012781.1:n.522+78A=