Canonical Allele Identifier: CA1465408617

Gene: GNRHR

Linked Data

• dbSNP Id: rs1731628611

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740084_67740087dup , CM000666.2:g.67740084_67740087dup	GRCh38
NC_000004.11:g.68605802_68605805dup , CM000666.1:g.68605802_68605805dup	GRCh37
NC_000004.10:g.68288397_68288400dup	NCBI36
NG_009293.1:g.21002_21005dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*395_*398dup MANE Select	ENSP00000226413.5:n.*395_*398dup
ENST00000226413.4:c.*395_*398dup	ENSP00000226413.4:n.*395_*398dup
NM_000406.2:c.*395_*398dup	NP_000397.1:n.*395_*398dup
NM_001012763.1:c.*504_*507dup	NP_001012781.1:n.*504_*507dup
NM_000406.3:c.*395_*398dup MANE Select	NP_000397.1:n.*395_*398dup
NM_001012763.2:c.*504_*507dup	NP_001012781.1:n.*504_*507dup