Canonical Allele Identifier: CA2521812642
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419863del , CM000663.2:g.165419863del GRCh38
NC_000001.10:g.165389100del , CM000663.1:g.165389100del GRCh37
NC_000001.9:g.163655724del NCBI36
NG_029517.1:g.30493del
NG_029517.2:g.30493del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.442+7del MANE Select ENSP00000352900.5:n.442+7del
ENST00000359842.9:c.442+7del ENSP00000352900.5:n.442+7del
ENST00000470566.1:n.367+7del
ENST00000619224.1:c.73+7del ENSP00000482458.1:n.73+7del
NM_001256570.1:c.73+7del NP_001243499.1:n.73+7del
NM_001256571.1:c.73+7del NP_001243500.1:n.73+7del
NM_006917.4:c.442+7del NP_008848.1:n.442+7del
NM_006917.5:c.442+7del MANE Select NP_008848.1:n.442+7del
NM_001256571.2:c.73+7del NP_001243500.1:n.73+7del
NM_001256570.2:c.73+7del NP_001243499.1:n.73+7del