Canonical Allele Identifier: CA2648887621
Gene: RXRG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419893_165419894del , CM000663.2:g.165419893_165419894del GRCh38
NC_000001.10:g.165389130_165389131del , CM000663.1:g.165389130_165389131del GRCh37
NC_000001.9:g.163655754_163655755del NCBI36
NG_029517.1:g.30462_30463del
NG_029517.2:g.30462_30463del

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.418_419del MANE Select ENSP00000352900.5:p.Ala140HisfsTer17
ENST00000359842.9:c.418_419del ENSP00000352900.5:p.Ala140HisfsTer17
ENST00000470566.1:n.343_344del
ENST00000619224.1:c.49_50del ENSP00000482458.1:p.Ala17HisfsTer17
NM_001256570.1:c.49_50del NP_001243499.1:p.Ala17HisfsTer17
NM_001256571.1:c.49_50del NP_001243500.1:p.Ala17HisfsTer17
NM_006917.4:c.418_419del NP_008848.1:p.Ala140HisfsTer17
NM_006917.5:c.418_419del MANE Select NP_008848.1:p.Ala140HisfsTer17
NM_001256571.2:c.49_50del NP_001243500.1:p.Ala17HisfsTer17
NM_001256570.2:c.49_50del NP_001243499.1:p.Ala17HisfsTer17