Canonical Allele Identifier: CA1465420486

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753840G= , CM000666.2:g.67753840G=	GRCh38
NC_000004.11:g.68619558G= , CM000666.1:g.68619558G=	GRCh37
NC_000004.10:g.68302153G=	NCBI36
NG_009293.1:g.7247C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.496C= MANE Select	ENSP00000226413.5:p.Leu166=
ENST00000226413.4:c.496C=	ENSP00000226413.4:p.Leu166=
ENST00000420975.2:c.496C=	ENSP00000397561.2:p.Leu166=
NM_000406.2:c.496C=	NP_000397.1:p.Leu166=
NM_001012763.1:c.496C=	NP_001012781.1:p.Leu166=
NM_000406.3:c.496C= MANE Select	NP_000397.1:p.Leu166=
NM_001012763.2:c.496C=	NP_001012781.1:p.Leu166=