Canonical Allele Identifier: CA2832528655
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754088del , CM000666.2:g.67754088del GRCh38
NC_000004.11:g.68619806del , CM000666.1:g.68619806del GRCh37
NC_000004.10:g.68302401del NCBI36
NG_009293.1:g.6999del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.248del MANE Select ENSP00000226413.5:p.Leu83ArgfsTer3
ENST00000226413.4:c.248del ENSP00000226413.4:p.Leu83ArgfsTer3
ENST00000420975.2:c.248del ENSP00000397561.2:p.Leu83ArgfsTer3
NM_000406.2:c.248del NP_000397.1:p.Leu83ArgfsTer3
NM_001012763.1:c.248del NP_001012781.1:p.Leu83ArgfsTer3
NM_000406.3:c.248del MANE Select NP_000397.1:p.Leu83ArgfsTer3
NM_001012763.2:c.248del NP_001012781.1:p.Leu83ArgfsTer3