Canonical Allele Identifier: CA1204419651

Gene: RXRG

Linked Data

• dbSNP Id: rs1658922122

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439711_165439713del , CM000663.2:g.165439711_165439713del	GRCh38
NC_000001.10:g.165408948_165408950del , CM000663.1:g.165408948_165408950del	GRCh37
NC_000001.9:g.163675572_163675574del	NCBI36
NG_029517.1:g.10645_10647del
NG_029517.2:g.10645_10647del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5134_49+5136del MANE Select	ENSP00000352900.5:n.49+5134_49+5136del
ENST00000359842.9:c.49+5134_49+5136del	ENSP00000352900.5:n.49+5134_49+5136del
ENST00000465764.1:n.329-2510_329-2508del
ENST00000619224.1:c.-379+5134_-379+5136del	ENSP00000482458.1:n.-379+5134_-379+5136del
NM_001256570.1:c.-379+5134_-379+5136del	NP_001243499.1:n.-379+5134_-379+5136del
NM_006917.4:c.49+5134_49+5136del	NP_008848.1:n.49+5134_49+5136del
NR_033824.1:n.512-2510_512-2508del
NM_006917.5:c.49+5134_49+5136del MANE Select	NP_008848.1:n.49+5134_49+5136del
NR_033824.2:n.283-2510_283-2508del
NM_001256570.2:c.-379+5134_-379+5136del	NP_001243499.1:n.-379+5134_-379+5136del