Canonical Allele Identifier: CA1204410217

Gene: RXRG

Linked Data

• dbSNP Id: rs1658264508
• gnomAD v4: 1-165420153-CCTAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420156_165420159del , CM000663.2:g.165420156_165420159del	GRCh38
NC_000001.10:g.165389393_165389396del , CM000663.1:g.165389393_165389396del	GRCh37
NC_000001.9:g.163656017_163656020del	NCBI36
NG_029517.1:g.30199_30202del
NG_029517.2:g.30199_30202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-143_298-140del MANE Select	ENSP00000352900.5:n.298-143_298-140del
ENST00000359842.9:c.298-143_298-140del	ENSP00000352900.5:n.298-143_298-140del
ENST00000470566.1:n.223-143_223-140del
ENST00000619224.1:c.-72-143_-72-140del	ENSP00000482458.1:n.-72-143_-72-140del
NM_001256570.1:c.-72-143_-72-140del	NP_001243499.1:n.-72-143_-72-140del
NM_001256571.1:c.-72-143_-72-140del	NP_001243500.1:n.-72-143_-72-140del
NM_006917.4:c.298-143_298-140del	NP_008848.1:n.298-143_298-140del
NM_006917.5:c.298-143_298-140del MANE Select	NP_008848.1:n.298-143_298-140del
NM_001256571.2:c.-72-143_-72-140del	NP_001243500.1:n.-72-143_-72-140del
NM_001256570.2:c.-72-143_-72-140del	NP_001243499.1:n.-72-143_-72-140del