Canonical Allele Identifier: CA1465420472

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753833C= , CM000666.2:g.67753833C=	GRCh38
NC_000004.11:g.68619551C= , CM000666.1:g.68619551C=	GRCh37
NC_000004.10:g.68302146C=	NCBI36
NG_009293.1:g.7254G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.503G= MANE Select	ENSP00000226413.5:p.Ser168=
ENST00000226413.4:c.503G=	ENSP00000226413.4:p.Ser168=
ENST00000420975.2:c.503G=	ENSP00000397561.2:p.Ser168=
NM_000406.2:c.503G=	NP_000397.1:p.Ser168=
NM_001012763.1:c.503G=	NP_001012781.1:p.Ser168=
NM_000406.3:c.503G= MANE Select	NP_000397.1:p.Ser168=
NM_001012763.2:c.503G=	NP_001012781.1:p.Ser168=