Canonical Allele Identifier: CA1465409035

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740526A= , CM000666.2:g.67740526A=	GRCh38
NC_000004.11:g.68606244A= , CM000666.1:g.68606244A=	GRCh37
NC_000004.10:g.68288839A=	NCBI36
NG_009293.1:g.20561T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.941T= MANE Select	ENSP00000226413.5:p.Leu314=
ENST00000226413.4:c.941T=	ENSP00000226413.4:p.Leu314=
ENST00000420975.2:c.813T=	ENSP00000397561.2:n.813T=
NM_000406.2:c.941T=	NP_000397.1:p.Leu314=
NM_001012763.1:c.*63T=	NP_001012781.1:n.*63T=
NM_000406.3:c.941T= MANE Select	NP_000397.1:p.Leu314=
NM_001012763.2:c.*63T=	NP_001012781.1:n.*63T=