Canonical Allele Identifier: CA2670819602

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740094-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740095del , CM000666.2:g.67740095del	GRCh38
NC_000004.11:g.68605813del , CM000666.1:g.68605813del	GRCh37
NC_000004.10:g.68288408del	NCBI36
NG_009293.1:g.20992del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*385del MANE Select	ENSP00000226413.5:n.*385del
ENST00000226413.4:c.*385del	ENSP00000226413.4:n.*385del
NM_000406.2:c.*385del	NP_000397.1:n.*385del
NM_001012763.1:c.*494del	NP_001012781.1:n.*494del
NM_000406.3:c.*385del MANE Select	NP_000397.1:n.*385del
NM_001012763.2:c.*494del	NP_001012781.1:n.*494del