Canonical Allele Identifier: CA1008697445

Gene: RXRG

Linked Data

• dbSNP Id: rs565597851
• gnomAD v3: 1-165419396-C-CTT
• gnomAD v4: 1-165419396-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419407_165419408dup , CM000663.2:g.165419407_165419408dup	GRCh38
NC_000001.10:g.165388644_165388645dup , CM000663.1:g.165388644_165388645dup	GRCh37
NC_000001.9:g.163655268_163655269dup	NCBI36
NG_029517.1:g.30958_30959dup
NG_029517.2:g.30958_30959dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+472_442+473dup MANE Select	ENSP00000352900.5:n.442+472_442+473dup
ENST00000359842.9:c.442+472_442+473dup	ENSP00000352900.5:n.442+472_442+473dup
ENST00000470566.1:n.367+472_367+473dup
ENST00000619224.1:c.73+472_73+473dup	ENSP00000482458.1:n.73+472_73+473dup
NM_001256570.1:c.73+472_73+473dup	NP_001243499.1:n.73+472_73+473dup
NM_001256571.1:c.73+472_73+473dup	NP_001243500.1:n.73+472_73+473dup
NM_006917.4:c.442+472_442+473dup	NP_008848.1:n.442+472_442+473dup
NM_006917.5:c.442+472_442+473dup MANE Select	NP_008848.1:n.442+472_442+473dup
NM_001256571.2:c.73+472_73+473dup	NP_001243500.1:n.73+472_73+473dup
NM_001256570.2:c.73+472_73+473dup	NP_001243499.1:n.73+472_73+473dup