Canonical Allele Identifier: CA2648887624
Gene: RXRG HGNC NCBI

Linked Data

gnomAD v4: 1-165419972-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419973del , CM000663.2:g.165419973del GRCh38
NC_000001.10:g.165389210del , CM000663.1:g.165389210del GRCh37
NC_000001.9:g.163655834del NCBI36
NG_029517.1:g.30383del
NG_029517.2:g.30383del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.339del MANE Select ENSP00000352900.5:p.Lys113AsnfsTer12
ENST00000359842.9:c.339del ENSP00000352900.5:p.Lys113AsnfsTer12
ENST00000470566.1:n.264del
ENST00000619224.1:c.-31del ENSP00000482458.1:n.-31del
NM_001256570.1:c.-31del NP_001243499.1:n.-31del
NM_001256571.1:c.-31del NP_001243500.1:n.-31del
NM_006917.4:c.339del NP_008848.1:p.Lys113AsnfsTer12
NM_006917.5:c.339del MANE Select NP_008848.1:p.Lys113AsnfsTer12
NM_001256571.2:c.-31del NP_001243500.1:n.-31del
NM_001256570.2:c.-31del NP_001243499.1:n.-31del
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