Canonical Allele Identifier: CA1204419754

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439856_165439857delinsAG , CM000663.2:g.165439856_165439857delinsAG	GRCh38
NC_000001.10:g.165409093_165409094delinsAG , CM000663.1:g.165409093_165409094delinsAG	GRCh37
NC_000001.9:g.163675717_163675718delinsAG	NCBI36
NG_029517.1:g.10499_10500delinsCT
NG_029517.2:g.10499_10500delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4988_49+4989delinsCT MANE Select	ENSP00000352900.5:n.49+4988_49+4989delinsCT
ENST00000359842.9:c.49+4988_49+4989delinsCT	ENSP00000352900.5:n.49+4988_49+4989delinsCT
ENST00000465764.1:n.329-2656_329-2655delinsCT
ENST00000619224.1:c.-379+4988_-379+4989delinsCT	ENSP00000482458.1:n.-379+4988_-379+4989delinsCT
NM_001256570.1:c.-379+4988_-379+4989delinsCT	NP_001243499.1:n.-379+4988_-379+4989delinsCT
NM_006917.4:c.49+4988_49+4989delinsCT	NP_008848.1:n.49+4988_49+4989delinsCT
NR_033824.1:n.512-2656_512-2655delinsCT
NM_006917.5:c.49+4988_49+4989delinsCT MANE Select	NP_008848.1:n.49+4988_49+4989delinsCT
NR_033824.2:n.283-2656_283-2655delinsCT
NM_001256570.2:c.-379+4988_-379+4989delinsCT	NP_001243499.1:n.-379+4988_-379+4989delinsCT