Canonical Allele Identifier: CA1204419713
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439796_165439798delinsAAC , CM000663.2:g.165439796_165439798delinsAAC GRCh38
NC_000001.10:g.165409033_165409035delinsAAC , CM000663.1:g.165409033_165409035delinsAAC GRCh37
NC_000001.9:g.163675657_163675659delinsAAC NCBI36
NG_029517.1:g.10558_10560delinsGTT
NG_029517.2:g.10558_10560delinsGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+5047_49+5049delinsGTT MANE Select ENSP00000352900.5:n.49+5047_49+5049delins...
ENST00000359842.9:c.49+5047_49+5049delinsGTT ENSP00000352900.5:n.49+5047_49+5049delins...
ENST00000465764.1:n.329-2597_329-2595delinsGTT
ENST00000619224.1:c.-379+5047_-379+5049delinsGTT ENSP00000482458.1:n.-379+5047_-379+5049de...
NM_001256570.1:c.-379+5047_-379+5049delinsGTT NP_001243499.1:n.-379+5047_-379+5049delin...
NM_006917.4:c.49+5047_49+5049delinsGTT NP_008848.1:n.49+5047_49+5049delinsGTT
NR_033824.1:n.512-2597_512-2595delinsGTT
NM_006917.5:c.49+5047_49+5049delinsGTT MANE Select NP_008848.1:n.49+5047_49+5049delinsGTT
NR_033824.2:n.283-2597_283-2595delinsGTT
NM_001256570.2:c.-379+5047_-379+5049delinsGTT NP_001243499.1:n.-379+5047_-379+5049delin...