Canonical Allele Identifier: CA1204410213
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165420150_165420151delinsCT , CM000663.2:g.165420150_165420151delinsCT GRCh38
NC_000001.10:g.165389387_165389388delinsCT , CM000663.1:g.165389387_165389388delinsCT GRCh37
NC_000001.9:g.163656011_163656012delinsCT NCBI36
NG_029517.1:g.30205_30206delinsAG
NG_029517.2:g.30205_30206delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.298-137_298-136delinsAG MANE Select ENSP00000352900.5:n.298-137_298-136delinsAG
ENST00000359842.9:c.298-137_298-136delinsAG ENSP00000352900.5:n.298-137_298-136delinsAG
ENST00000470566.1:n.223-137_223-136delinsAG
ENST00000619224.1:c.-72-137_-72-136delinsAG ENSP00000482458.1:n.-72-137_-72-136delinsAG
NM_001256570.1:c.-72-137_-72-136delinsAG NP_001243499.1:n.-72-137_-72-136delinsAG
NM_001256571.1:c.-72-137_-72-136delinsAG NP_001243500.1:n.-72-137_-72-136delinsAG
NM_006917.4:c.298-137_298-136delinsAG NP_008848.1:n.298-137_298-136delinsAG
NM_006917.5:c.298-137_298-136delinsAG MANE Select NP_008848.1:n.298-137_298-136delinsAG
NM_001256571.2:c.-72-137_-72-136delinsAG NP_001243500.1:n.-72-137_-72-136delinsAG
NM_001256570.2:c.-72-137_-72-136delinsAG NP_001243499.1:n.-72-137_-72-136delinsAG