Canonical Allele Identifier: CA2670819720
Gene: GNRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740348del , CM000666.2:g.67740348del GRCh38
NC_000004.11:g.68606066del , CM000666.1:g.68606066del GRCh37
NC_000004.10:g.68288661del NCBI36
NG_009293.1:g.20742del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*135del MANE Select ENSP00000226413.5:n.*135del
ENST00000226413.4:c.*135del ENSP00000226413.4:n.*135del
NM_000406.2:c.*135del NP_000397.1:n.*135del
NM_001012763.1:c.*244del NP_001012781.1:n.*244del
NM_000406.3:c.*135del MANE Select NP_000397.1:n.*135del
NM_001012763.2:c.*244del NP_001012781.1:n.*244del