Canonical Allele Identifier: CA2648887697
Gene: RXRG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165420087dup , CM000663.2:g.165420087dup GRCh38
NC_000001.10:g.165389324dup , CM000663.1:g.165389324dup GRCh37
NC_000001.9:g.163655948dup NCBI36
NG_029517.1:g.30271dup
NG_029517.2:g.30271dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.298-71dup MANE Select ENSP00000352900.5:n.298-71dup
ENST00000359842.9:c.298-71dup ENSP00000352900.5:n.298-71dup
ENST00000470566.1:n.223-71dup
ENST00000619224.1:c.-72-71dup ENSP00000482458.1:n.-72-71dup
NM_001256570.1:c.-72-71dup NP_001243499.1:n.-72-71dup
NM_001256571.1:c.-72-71dup NP_001243500.1:n.-72-71dup
NM_006917.4:c.298-71dup NP_008848.1:n.298-71dup
NM_006917.5:c.298-71dup MANE Select NP_008848.1:n.298-71dup
NM_001256571.2:c.-72-71dup NP_001243500.1:n.-72-71dup
NM_001256570.2:c.-72-71dup NP_001243499.1:n.-72-71dup