Canonical Allele Identifier: CA2522396109
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740693_67740698del , CM000666.2:g.67740693_67740698del GRCh38
NC_000004.11:g.68606411_68606416del , CM000666.1:g.68606411_68606416del GRCh37
NC_000004.10:g.68289006_68289011del NCBI36
NG_009293.1:g.20389_20394del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.769_774del MANE Select ENSP00000226413.5:p.Asn257_Ile258del
ENST00000226413.4:c.769_774del ENSP00000226413.4:p.Asn257_Ile258del
ENST00000420975.2:c.641_646del ENSP00000397561.2:p.Gln214_Thr216delinsPro
NM_000406.2:c.769_774del NP_000397.1:p.Asn257_Ile258del
NM_001012763.1:c.641_646del NP_001012781.1:p.Gln214_Thr216delinsPro
NM_000406.3:c.769_774del MANE Select NP_000397.1:p.Asn257_Ile258del
NM_001012763.2:c.641_646del NP_001012781.1:p.Gln214_Thr216delinsPro
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