Canonical Allele Identifier: CA1465420969

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754216C= , CM000666.2:g.67754216C=	GRCh38
NC_000004.11:g.68619934C= , CM000666.1:g.68619934C=	GRCh37
NC_000004.10:g.68302529C=	NCBI36
NG_009293.1:g.6871G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.120G= MANE Select	ENSP00000226413.5:p.Thr40=
ENST00000226413.4:c.120G=	ENSP00000226413.4:p.Thr40=
ENST00000420975.2:c.120G=	ENSP00000397561.2:p.Thr40=
NM_000406.2:c.120G=	NP_000397.1:p.Thr40=
NM_001012763.1:c.120G=	NP_001012781.1:p.Thr40=
NM_000406.3:c.120G= MANE Select	NP_000397.1:p.Thr40=
NM_001012763.2:c.120G=	NP_001012781.1:p.Thr40=