Canonical Allele Identifier: CA1465409166

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740664A= , CM000666.2:g.67740664A=	GRCh38
NC_000004.11:g.68606382A= , CM000666.1:g.68606382A=	GRCh37
NC_000004.10:g.68288977A=	NCBI36
NG_009293.1:g.20423T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.803T= MANE Select	ENSP00000226413.5:p.Met268=
ENST00000226413.4:c.803T=	ENSP00000226413.4:p.Met268=
ENST00000420975.2:c.675T=	ENSP00000397561.2:p.Asn225=
NM_000406.2:c.803T=	NP_000397.1:p.Met268=
NM_001012763.1:c.675T=	NP_001012781.1:p.Asn225=
NM_000406.3:c.803T= MANE Select	NP_000397.1:p.Met268=
NM_001012763.2:c.675T=	NP_001012781.1:p.Asn225=