Canonical Allele Identifier: CA1204410216
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165420153_165420157delinsCCTAT , CM000663.2:g.165420153_165420157delinsCCTAT GRCh38
NC_000001.10:g.165389390_165389394delinsCCTAT , CM000663.1:g.165389390_165389394delinsCCTAT GRCh37
NC_000001.9:g.163656014_163656018delinsCCTAT NCBI36
NG_029517.1:g.30199_30203delinsATAGG
NG_029517.2:g.30199_30203delinsATAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.298-143_298-139delinsATAGG MANE Select ENSP00000352900.5:n.298-143_298-139delinsATAGG
ENST00000359842.9:c.298-143_298-139delinsATAGG ENSP00000352900.5:n.298-143_298-139delinsATAGG
ENST00000470566.1:n.223-143_223-139delinsATAGG
ENST00000619224.1:c.-72-143_-72-139delinsATAGG ENSP00000482458.1:n.-72-143_-72-139delinsATAGG
NM_001256570.1:c.-72-143_-72-139delinsATAGG NP_001243499.1:n.-72-143_-72-139delinsATAGG
NM_001256571.1:c.-72-143_-72-139delinsATAGG NP_001243500.1:n.-72-143_-72-139delinsATAGG
NM_006917.4:c.298-143_298-139delinsATAGG NP_008848.1:n.298-143_298-139delinsATAGG
NM_006917.5:c.298-143_298-139delinsATAGG MANE Select NP_008848.1:n.298-143_298-139delinsATAGG
NM_001256571.2:c.-72-143_-72-139delinsATAGG NP_001243500.1:n.-72-143_-72-139delinsATAGG
NM_001256570.2:c.-72-143_-72-139delinsATAGG NP_001243499.1:n.-72-143_-72-139delinsATAGG