Canonical Allele Identifier: CA1465420493

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753846A= , CM000666.2:g.67753846A=	GRCh38
NC_000004.11:g.68619564A= , CM000666.1:g.68619564A=	GRCh37
NC_000004.10:g.68302159A=	NCBI36
NG_009293.1:g.7241T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.490T= MANE Select	ENSP00000226413.5:p.Trp164=
ENST00000226413.4:c.490T=	ENSP00000226413.4:p.Trp164=
ENST00000420975.2:c.490T=	ENSP00000397561.2:p.Trp164=
NM_000406.2:c.490T=	NP_000397.1:p.Trp164=
NM_001012763.1:c.490T=	NP_001012781.1:p.Trp164=
NM_000406.3:c.490T= MANE Select	NP_000397.1:p.Trp164=
NM_001012763.2:c.490T=	NP_001012781.1:p.Trp164=