Canonical Allele Identifier: CA1465409196
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731642338
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740673_67740678del , CM000666.2:g.67740673_67740678del GRCh38
NC_000004.11:g.68606391_68606396del , CM000666.1:g.68606391_68606396del GRCh37
NC_000004.10:g.68288986_68288991del NCBI36
NG_009293.1:g.20409_20414del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.789_794del MANE Select ENSP00000226413.5:p.Lys264_Thr265del
ENST00000226413.4:c.789_794del ENSP00000226413.4:p.Lys264_Thr265del
ENST00000420975.2:c.661_666del ENSP00000397561.2:p.Glu221_Asp222del
NM_000406.2:c.789_794del NP_000397.1:p.Lys264_Thr265del
NM_001012763.1:c.661_666del NP_001012781.1:p.Glu221_Asp222del
NM_000406.3:c.789_794del MANE Select NP_000397.1:p.Lys264_Thr265del
NM_001012763.2:c.661_666del NP_001012781.1:p.Glu221_Asp222del
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