Canonical Allele Identifier: CA1008697685

Gene: RXRG

Linked Data

• dbSNP Id: rs1658257126
• gnomAD v3: 1-165419964-T-TG
• gnomAD v4: 1-165419964-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419966dup , CM000663.2:g.165419966dup	GRCh38
NC_000001.10:g.165389203dup , CM000663.1:g.165389203dup	GRCh37
NC_000001.9:g.163655827dup	NCBI36
NG_029517.1:g.30391dup
NG_029517.2:g.30391dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.347dup MANE Select	ENSP00000352900.5:p.Gly117ArgfsTer20
ENST00000359842.9:c.347dup	ENSP00000352900.5:p.Gly117ArgfsTer20
ENST00000470566.1:n.272dup
ENST00000619224.1:c.-23dup	ENSP00000482458.1:n.-23dup
NM_001256570.1:c.-23dup	NP_001243499.1:n.-23dup
NM_001256571.1:c.-23dup	NP_001243500.1:n.-23dup
NM_006917.4:c.347dup	NP_008848.1:p.Gly117ArgfsTer20
NM_006917.5:c.347dup MANE Select	NP_008848.1:p.Gly117ArgfsTer20
NM_001256571.2:c.-23dup	NP_001243500.1:n.-23dup
NM_001256570.2:c.-23dup	NP_001243499.1:n.-23dup