Canonical Allele Identifier: CA527077795

Gene: RXRG

Linked Data

• dbSNP Id: rs565597851
• gnomAD v2: 1-165388633-CTT-C
• gnomAD v3: 1-165419396-CTT-C
• gnomAD v4: 1-165419396-CTT-C
• MyVariant Identifiers: chr1:g.165388634_165388635del (hg19) ; chr1:g.165419397_165419398del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419407_165419408del , CM000663.2:g.165419407_165419408del	GRCh38
NC_000001.10:g.165388644_165388645del , CM000663.1:g.165388644_165388645del	GRCh37
NC_000001.9:g.163655268_163655269del	NCBI36
NG_029517.1:g.30958_30959del
NG_029517.2:g.30958_30959del

Transcript Alleles

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