Canonical Allele Identifier: CA890557428
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1226453052

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439683_165439685del , CM000663.2:g.165439683_165439685del GRCh38
NC_000001.10:g.165408920_165408922del , CM000663.1:g.165408920_165408922del GRCh37
NC_000001.9:g.163675544_163675546del NCBI36
NG_029517.1:g.10673_10675del
NG_029517.2:g.10673_10675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.49+5162_49+5164del MANE Select ENSP00000352900.5:n.49+5162_49+5164del
ENST00000359842.9:c.49+5162_49+5164del ENSP00000352900.5:n.49+5162_49+5164del
ENST00000465764.1:n.329-2482_329-2480del
ENST00000619224.1:c.-379+5162_-379+5164del ENSP00000482458.1:n.-379+5162_-379+5164del
NM_001256570.1:c.-379+5162_-379+5164del NP_001243499.1:n.-379+5162_-379+5164del
NM_006917.4:c.49+5162_49+5164del NP_008848.1:n.49+5162_49+5164del
NR_033824.1:n.512-2482_512-2480del
NM_006917.5:c.49+5162_49+5164del MANE Select NP_008848.1:n.49+5162_49+5164del
NR_033824.2:n.283-2482_283-2480del
NM_001256570.2:c.-379+5162_-379+5164del NP_001243499.1:n.-379+5162_-379+5164del