Canonical Allele Identifier: CA1204409966

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419461_165419462delinsGC , CM000663.2:g.165419461_165419462delinsGC	GRCh38
NC_000001.10:g.165388698_165388699delinsGC , CM000663.1:g.165388698_165388699delinsGC	GRCh37
NC_000001.9:g.163655322_163655323delinsGC	NCBI36
NG_029517.1:g.30894_30895delinsGC
NG_029517.2:g.30894_30895delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+408_442+409delinsGC MANE Select	ENSP00000352900.5:n.442+408_442+409delinsGC
ENST00000359842.9:c.442+408_442+409delinsGC	ENSP00000352900.5:n.442+408_442+409delinsGC
ENST00000470566.1:n.367+408_367+409delinsGC
ENST00000619224.1:c.73+408_73+409delinsGC	ENSP00000482458.1:n.73+408_73+409delinsGC
NM_001256570.1:c.73+408_73+409delinsGC	NP_001243499.1:n.73+408_73+409delinsGC
NM_001256571.1:c.73+408_73+409delinsGC	NP_001243500.1:n.73+408_73+409delinsGC
NM_006917.4:c.442+408_442+409delinsGC	NP_008848.1:n.442+408_442+409delinsGC
NM_006917.5:c.442+408_442+409delinsGC MANE Select	NP_008848.1:n.442+408_442+409delinsGC
NM_001256571.2:c.73+408_73+409delinsGC	NP_001243500.1:n.73+408_73+409delinsGC
NM_001256570.2:c.73+408_73+409delinsGC	NP_001243499.1:n.73+408_73+409delinsGC