Canonical Allele Identifier: CA1204409994

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419541_165419543delinsCTG , CM000663.2:g.165419541_165419543delinsCTG	GRCh38
NC_000001.10:g.165388778_165388780delinsCTG , CM000663.1:g.165388778_165388780delinsCTG	GRCh37
NC_000001.9:g.163655402_163655404delinsCTG	NCBI36
NG_029517.1:g.30813_30815delinsCAG
NG_029517.2:g.30813_30815delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+327_442+329delinsCAG MANE Select	ENSP00000352900.5:n.442+327_442+329delinsCAG
ENST00000359842.9:c.442+327_442+329delinsCAG	ENSP00000352900.5:n.442+327_442+329delinsCAG
ENST00000470566.1:n.367+327_367+329delinsCAG
ENST00000619224.1:c.73+327_73+329delinsCAG	ENSP00000482458.1:n.73+327_73+329delinsCAG
NM_001256570.1:c.73+327_73+329delinsCAG	NP_001243499.1:n.73+327_73+329delinsCAG
NM_001256571.1:c.73+327_73+329delinsCAG	NP_001243500.1:n.73+327_73+329delinsCAG
NM_006917.4:c.442+327_442+329delinsCAG	NP_008848.1:n.442+327_442+329delinsCAG
NM_006917.5:c.442+327_442+329delinsCAG MANE Select	NP_008848.1:n.442+327_442+329delinsCAG
NM_001256571.2:c.73+327_73+329delinsCAG	NP_001243500.1:n.73+327_73+329delinsCAG
NM_001256570.2:c.73+327_73+329delinsCAG	NP_001243499.1:n.73+327_73+329delinsCAG