Canonical Allele Identifier: CA2762037074

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740140_67740146del , CM000666.2:g.67740140_67740146del	GRCh38
NC_000004.11:g.68605858_68605864del , CM000666.1:g.68605858_68605864del	GRCh37
NC_000004.10:g.68288453_68288459del	NCBI36
NG_009293.1:g.20941_20947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*334_*340del MANE Select	ENSP00000226413.5:n.*334_*340del
ENST00000226413.4:c.*334_*340del	ENSP00000226413.4:n.*334_*340del
NM_000406.2:c.*334_*340del	NP_000397.1:n.*334_*340del
NM_001012763.1:c.*443_*449del	NP_001012781.1:n.*443_*449del
NM_000406.3:c.*334_*340del MANE Select	NP_000397.1:n.*334_*340del
NM_001012763.2:c.*443_*449del	NP_001012781.1:n.*443_*449del