Canonical Allele Identifier: CA1465420489

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753845C= , CM000666.2:g.67753845C=	GRCh38
NC_000004.11:g.68619563C= , CM000666.1:g.68619563C=	GRCh37
NC_000004.10:g.68302158C=	NCBI36
NG_009293.1:g.7242G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.491G= MANE Select	ENSP00000226413.5:p.Trp164=
ENST00000226413.4:c.491G=	ENSP00000226413.4:p.Trp164=
ENST00000420975.2:c.491G=	ENSP00000397561.2:p.Trp164=
NM_000406.2:c.491G=	NP_000397.1:p.Trp164=
NM_001012763.1:c.491G=	NP_001012781.1:p.Trp164=
NM_000406.3:c.491G= MANE Select	NP_000397.1:p.Trp164=
NM_001012763.2:c.491G=	NP_001012781.1:p.Trp164=