Canonical Allele Identifier: CA1140556290
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439857_165439858delinsGG , CM000663.2:g.165439857_165439858delinsGG GRCh38
NC_000001.10:g.165409094_165409095delinsGG , CM000663.1:g.165409094_165409095delinsGG GRCh37
NC_000001.9:g.163675718_163675719delinsGG NCBI36
NG_029517.1:g.10498_10499delinsCC
NG_029517.2:g.10498_10499delinsCC

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4987_49+4988delinsCC MANE Select ENSP00000352900.5:n.49+4987_49+4988delins...
ENST00000359842.9:c.49+4987_49+4988delinsCC ENSP00000352900.5:n.49+4987_49+4988delins...
ENST00000465764.1:n.329-2657_329-2656delinsCC
ENST00000619224.1:c.-379+4987_-379+4988delinsCC ENSP00000482458.1:n.-379+4987_-379+4988de...
NM_001256570.1:c.-379+4987_-379+4988delinsCC NP_001243499.1:n.-379+4987_-379+4988delin...
NM_006917.4:c.49+4987_49+4988delinsCC NP_008848.1:n.49+4987_49+4988delinsCC
NR_033824.1:n.512-2657_512-2656delinsCC
NM_006917.5:c.49+4987_49+4988delinsCC MANE Select NP_008848.1:n.49+4987_49+4988delinsCC
NR_033824.2:n.283-2657_283-2656delinsCC
NM_001256570.2:c.-379+4987_-379+4988delinsCC NP_001243499.1:n.-379+4987_-379+4988delin...