Canonical Allele Identifier: CA1204419897

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165440005_165440006delinsAG , CM000663.2:g.165440005_165440006delinsAG	GRCh38
NC_000001.10:g.165409242_165409243delinsAG , CM000663.1:g.165409242_165409243delinsAG	GRCh37
NC_000001.9:g.163675866_163675867delinsAG	NCBI36
NG_029517.1:g.10350_10351delinsCT
NG_029517.2:g.10350_10351delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4839_49+4840delinsCT MANE Select	ENSP00000352900.5:n.49+4839_49+4840delinsCT
ENST00000359842.9:c.49+4839_49+4840delinsCT	ENSP00000352900.5:n.49+4839_49+4840delinsCT
ENST00000465764.1:n.329-2805_329-2804delinsCT
ENST00000619224.1:c.-379+4839_-379+4840delinsCT	ENSP00000482458.1:n.-379+4839_-379+4840delinsCT
NM_001256570.1:c.-379+4839_-379+4840delinsCT	NP_001243499.1:n.-379+4839_-379+4840delinsCT
NM_006917.4:c.49+4839_49+4840delinsCT	NP_008848.1:n.49+4839_49+4840delinsCT
NR_033824.1:n.512-2805_512-2804delinsCT
NM_006917.5:c.49+4839_49+4840delinsCT MANE Select	NP_008848.1:n.49+4839_49+4840delinsCT
NR_033824.2:n.283-2805_283-2804delinsCT
NM_001256570.2:c.-379+4839_-379+4840delinsCT	NP_001243499.1:n.-379+4839_-379+4840delinsCT