Canonical Allele Identifier: CA1465409185
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740670_67740671delinsAG , CM000666.2:g.67740670_67740671delinsAG GRCh38
NC_000004.11:g.68606388_68606389delinsAG , CM000666.1:g.68606388_68606389delinsAG GRCh37
NC_000004.10:g.68288983_68288984delinsAG NCBI36
NG_009293.1:g.20416_20417delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.796_797delinsCT MANE Select ENSP00000226413.5:p.Leu266=
ENST00000226413.4:c.796_797delinsCT ENSP00000226413.4:p.Leu266=
ENST00000420975.2:c.668_669delinsCT ENSP00000397561.2:p.Ser223=
NM_000406.2:c.796_797delinsCT NP_000397.1:p.Leu266=
NM_001012763.1:c.668_669delinsCT NP_001012781.1:p.Ser223=
NM_000406.3:c.796_797delinsCT MANE Select NP_000397.1:p.Leu266=
NM_001012763.2:c.668_669delinsCT NP_001012781.1:p.Ser223=
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