Canonical Allele Identifier: CA1008697457

Gene: RXRG

Linked Data

• gnomAD v3: 1-165419408-TGA-T
• gnomAD v4: 1-165419408-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419411_165419412del , CM000663.2:g.165419411_165419412del	GRCh38
NC_000001.10:g.165388648_165388649del , CM000663.1:g.165388648_165388649del	GRCh37
NC_000001.9:g.163655272_163655273del	NCBI36
NG_029517.1:g.30946_30947del
NG_029517.2:g.30946_30947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+460_442+461del MANE Select	ENSP00000352900.5:n.442+460_442+461del
ENST00000359842.9:c.442+460_442+461del	ENSP00000352900.5:n.442+460_442+461del
ENST00000470566.1:n.367+460_367+461del
ENST00000619224.1:c.73+460_73+461del	ENSP00000482458.1:n.73+460_73+461del
NM_001256570.1:c.73+460_73+461del	NP_001243499.1:n.73+460_73+461del
NM_001256571.1:c.73+460_73+461del	NP_001243500.1:n.73+460_73+461del
NM_006917.4:c.442+460_442+461del	NP_008848.1:n.442+460_442+461del
NM_006917.5:c.442+460_442+461del MANE Select	NP_008848.1:n.442+460_442+461del
NM_001256571.2:c.73+460_73+461del	NP_001243500.1:n.73+460_73+461del
NM_001256570.2:c.73+460_73+461del	NP_001243499.1:n.73+460_73+461del