Canonical Allele Identifier: CA649016701

Gene: GNRHR

Linked Data

• COSMIC: COSN17663519

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740186_67740187insC , CM000666.2:g.67740186_67740187insC	GRCh38
NC_000004.11:g.68605904_68605905insC , CM000666.1:g.68605904_68605905insC	GRCh37
NC_000004.10:g.68288499_68288500insC	NCBI36
NG_009293.1:g.20900_20901insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*293_*294insG MANE Select	ENSP00000226413.5:n.*293_*294insG
ENST00000226413.4:c.*293_*294insG	ENSP00000226413.4:n.*293_*294insG
NM_000406.2:c.*293_*294insG	NP_000397.1:n.*293_*294insG
NM_001012763.1:c.*402_*403insG	NP_001012781.1:n.*402_*403insG
NM_000406.3:c.*293_*294insG MANE Select	NP_000397.1:n.*293_*294insG
NM_001012763.2:c.*402_*403insG	NP_001012781.1:n.*402_*403insG