Canonical Allele Identifier: CA1465409194
Gene: GNRHR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740672_67740678delinsAGTCTTC , CM000666.2:g.67740672_67740678delinsAGTCTTC GRCh38
NC_000004.11:g.68606390_68606396delinsAGTCTTC , CM000666.1:g.68606390_68606396delinsAGTCTTC GRCh37
NC_000004.10:g.68288985_68288991delinsAGTCTTC NCBI36
NG_009293.1:g.20409_20415delinsGAAGACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.789_795delinsGAAGACT MANE Select ENSP00000226413.5:p.Leu263=
ENST00000226413.4:c.789_795delinsGAAGACT ENSP00000226413.4:p.Leu263=
ENST00000420975.2:c.661_667delinsGAAGACT ENSP00000397561.2:p.Glu221=
NM_000406.2:c.789_795delinsGAAGACT NP_000397.1:p.Leu263=
NM_001012763.1:c.661_667delinsGAAGACT NP_001012781.1:p.Glu221=
NM_000406.3:c.789_795delinsGAAGACT MANE Select NP_000397.1:p.Leu263=
NM_001012763.2:c.661_667delinsGAAGACT NP_001012781.1:p.Glu221=
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