Canonical Allele Identifier: CA1465409066
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740569A= , CM000666.2:g.67740569A= GRCh38
NC_000004.11:g.68606287A= , CM000666.1:g.68606287A= GRCh37
NC_000004.10:g.68288882A= NCBI36
NG_009293.1:g.20518T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.898T= MANE Select ENSP00000226413.5:p.Leu300=
ENST00000226413.4:c.898T= ENSP00000226413.4:p.Leu300=
ENST00000420975.2:c.770T= ENSP00000397561.2:n.770T=
NM_000406.2:c.898T= NP_000397.1:p.Leu300=
NM_001012763.1:c.*20T= NP_001012781.1:n.*20T=
NM_000406.3:c.898T= MANE Select NP_000397.1:p.Leu300=
NM_001012763.2:c.*20T= NP_001012781.1:n.*20T=
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