Canonical Allele Identifier: CA1465409275

Gene: GNRHR

Linked Data

• dbSNP Id: rs1731643648

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740711_67740712insAATGTTAAACAGG , CM000666.2:g.67740711_67740712insAATGTTAAACAGG	GRCh38
NC_000004.11:g.68606429_68606430insAATGTTAAACAGG , CM000666.1:g.68606429_68606430insAATGTTAAACAGG	GRCh37
NC_000004.10:g.68289024_68289025insAATGTTAAACAGG	NCBI36
NG_009293.1:g.20375_20376insCCTGTTTAACATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.755_756insCCTGTTTAACATT MANE Select	ENSP00000226413.5:p.Gln253LeufsTer?
ENST00000226413.4:c.755_756insCCTGTTTAACATT	ENSP00000226413.4:p.Gln253LeufsTer?
ENST00000420975.2:c.627_628insCCTGTTTAACATT	ENSP00000397561.2:p.Ser210ProfsTer3
NM_000406.2:c.755_756insCCTGTTTAACATT	NP_000397.1:p.Gln253LeufsTer?
NM_001012763.1:c.627_628insCCTGTTTAACATT	NP_001012781.1:p.Ser210ProfsTer3
NM_000406.3:c.755_756insCCTGTTTAACATT MANE Select	NP_000397.1:p.Gln253LeufsTer?
NM_001012763.2:c.627_628insCCTGTTTAACATT	NP_001012781.1:p.Ser210ProfsTer3