Canonical Allele Identifier: CA1220224

Gene: RXRG

Linked Data

• dbSNP Id: rs747253200
• ExAC: 1:165389270 CTGT / C
• gnomAD v2: 1-165389270-CTGT-C
• gnomAD v4: 1-165420033-CTGT-C
• MyVariant Identifiers: chr1:g.165389271_165389273del (hg19) ; chr1:g.165420034_165420036del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420034_165420036del , CM000663.2:g.165420034_165420036del	GRCh38
NC_000001.10:g.165389271_165389273del , CM000663.1:g.165389271_165389273del	GRCh37
NC_000001.9:g.163655895_163655897del	NCBI36
NG_029517.1:g.30320_30322del
NG_029517.2:g.30320_30322del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-22_298-20del MANE Select	ENSP00000352900.5:n.298-22_298-20del
ENST00000359842.9:c.298-22_298-20del	ENSP00000352900.5:n.298-22_298-20del
ENST00000470566.1:n.223-22_223-20del
ENST00000619224.1:c.-72-22_-72-20del	ENSP00000482458.1:n.-72-22_-72-20del
NM_001256570.1:c.-72-22_-72-20del	NP_001243499.1:n.-72-22_-72-20del
NM_001256571.1:c.-72-22_-72-20del	NP_001243500.1:n.-72-22_-72-20del
NM_006917.4:c.298-22_298-20del	NP_008848.1:n.298-22_298-20del
NM_006917.5:c.298-22_298-20del MANE Select	NP_008848.1:n.298-22_298-20del
NM_001256571.2:c.-72-22_-72-20del	NP_001243500.1:n.-72-22_-72-20del
NM_001256570.2:c.-72-22_-72-20del	NP_001243499.1:n.-72-22_-72-20del