Canonical Allele Identifier: CA2670819675

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740240-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740244dup , CM000666.2:g.67740244dup	GRCh38
NC_000004.11:g.68605962dup , CM000666.1:g.68605962dup	GRCh37
NC_000004.10:g.68288557dup	NCBI36
NG_009293.1:g.20846dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*239dup MANE Select	ENSP00000226413.5:n.*239dup
ENST00000226413.4:c.*239dup	ENSP00000226413.4:n.*239dup
NM_000406.2:c.*239dup	NP_000397.1:n.*239dup
NM_001012763.1:c.*348dup	NP_001012781.1:n.*348dup
NM_000406.3:c.*239dup MANE Select	NP_000397.1:n.*239dup
NM_001012763.2:c.*348dup	NP_001012781.1:n.*348dup