Canonical Allele Identifier: CA2670819809
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740685-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740686del , CM000666.2:g.67740686del GRCh38
NC_000004.11:g.68606404del , CM000666.1:g.68606404del GRCh37
NC_000004.10:g.68288999del NCBI36
NG_009293.1:g.20401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.781del MANE Select ENSP00000226413.5:p.Ala261HisfsTer3
ENST00000226413.4:c.781del ENSP00000226413.4:p.Ala261HisfsTer3
ENST00000420975.2:c.653del ENSP00000397561.2:p.Ser218ThrfsTer?
NM_000406.2:c.781del NP_000397.1:p.Ala261HisfsTer3
NM_001012763.1:c.653del NP_001012781.1:p.Ser218ThrfsTer?
NM_000406.3:c.781del MANE Select NP_000397.1:p.Ala261HisfsTer3
NM_001012763.2:c.653del NP_001012781.1:p.Ser218ThrfsTer?
Search 100 bp 5'
Search 100 bp 3'