Canonical Allele Identifier: CA645518042
Gene: GNRHR HGNC NCBI

Linked Data

COSMIC: COSM391986
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754152_67754154del , CM000666.2:g.67754152_67754154del GRCh38
NC_000004.11:g.68619870_68619872del , CM000666.1:g.68619870_68619872del GRCh37
NC_000004.10:g.68302465_68302467del NCBI36
NG_009293.1:g.6935_6937del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.184_186del MANE Select ENSP00000226413.5:p.Lys62del
ENST00000226413.4:c.184_186del ENSP00000226413.4:p.Lys62del
ENST00000420975.2:c.184_186del ENSP00000397561.2:p.Lys62del
NM_000406.2:c.184_186del NP_000397.1:p.Lys62del
NM_001012763.1:c.184_186del NP_001012781.1:p.Lys62del
NM_000406.3:c.184_186del MANE Select NP_000397.1:p.Lys62del
NM_001012763.2:c.184_186del NP_001012781.1:p.Lys62del
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Search 100 bp 3'