Canonical Allele Identifier: CA2648887623
Gene: RXRG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419965_165419974del , CM000663.2:g.165419965_165419974del GRCh38
NC_000001.10:g.165389202_165389211del , CM000663.1:g.165389202_165389211del GRCh37
NC_000001.9:g.163655826_163655835del NCBI36
NG_029517.1:g.30384_30393del
NG_029517.2:g.30384_30393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.340_349del MANE Select ENSP00000352900.5:p.Pro114GlyfsTer8
ENST00000359842.9:c.340_349del ENSP00000352900.5:p.Pro114GlyfsTer8
ENST00000470566.1:n.265_274del
ENST00000619224.1:c.-30_-21del ENSP00000482458.1:n.-30_-21del
NM_001256570.1:c.-30_-21del NP_001243499.1:n.-30_-21del
NM_001256571.1:c.-30_-21del NP_001243500.1:n.-30_-21del
NM_006917.4:c.340_349del NP_008848.1:p.Pro114GlyfsTer8
NM_006917.5:c.340_349del MANE Select NP_008848.1:p.Pro114GlyfsTer8
NM_001256571.2:c.-30_-21del NP_001243500.1:n.-30_-21del
NM_001256570.2:c.-30_-21del NP_001243499.1:n.-30_-21del