Canonical Allele Identifier: CA1465409031

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740518A= , CM000666.2:g.67740518A=	GRCh38
NC_000004.11:g.68606236A= , CM000666.1:g.68606236A=	GRCh37
NC_000004.10:g.68288831A=	NCBI36
NG_009293.1:g.20569T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.949T= MANE Select	ENSP00000226413.5:p.Cys317=
ENST00000226413.4:c.949T=	ENSP00000226413.4:p.Cys317=
ENST00000420975.2:c.821T=	ENSP00000397561.2:n.821T=
NM_000406.2:c.949T=	NP_000397.1:p.Cys317=
NM_001012763.1:c.*71T=	NP_001012781.1:n.*71T=
NM_000406.3:c.949T= MANE Select	NP_000397.1:p.Cys317=
NM_001012763.2:c.*71T=	NP_001012781.1:n.*71T=