Canonical Allele Identifier: CA1465409175
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740669_67740671delinsTAG , CM000666.2:g.67740669_67740671delinsTAG GRCh38
NC_000004.11:g.68606387_68606389delinsTAG , CM000666.1:g.68606387_68606389delinsTAG GRCh37
NC_000004.10:g.68288982_68288984delinsTAG NCBI36
NG_009293.1:g.20416_20418delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.796_798delinsCTA MANE Select ENSP00000226413.5:p.Leu266=
ENST00000226413.4:c.796_798delinsCTA ENSP00000226413.4:p.Leu266=
ENST00000420975.2:c.668_670delinsCTA ENSP00000397561.2:p.Ser223=
NM_000406.2:c.796_798delinsCTA NP_000397.1:p.Leu266=
NM_001012763.1:c.668_670delinsCTA NP_001012781.1:p.Ser223=
NM_000406.3:c.796_798delinsCTA MANE Select NP_000397.1:p.Leu266=
NM_001012763.2:c.668_670delinsCTA NP_001012781.1:p.Ser223=