Canonical Allele Identifier: CA527077801

Gene: RXRG

Linked Data

• dbSNP Id: rs1233326227
• gnomAD v2: 1-165388765-C-CTACACCAAAGCACTGGGAT
• gnomAD v3: 1-165419528-C-CTACACCAAAGCACTGGGAT
• gnomAD v4: 1-165419528-C-CTACACCAAAGCACTGGGAT
• MyVariant Identifiers: chr1:g.165388765_165388766insTACACCAAAGCACTGGGAT (hg19) ; chr1:g.165419528_165419529insTACACCAAAGCACTGGGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419531_165419549dup , CM000663.2:g.165419531_165419549dup	GRCh38
NC_000001.10:g.165388768_165388786dup , CM000663.1:g.165388768_165388786dup	GRCh37
NC_000001.9:g.163655392_163655410dup	NCBI36
NG_029517.1:g.30809_30827dup
NG_029517.2:g.30809_30827dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+323_442+341dup MANE Select	ENSP00000352900.5:n.442+323_442+341dup
ENST00000359842.9:c.442+323_442+341dup	ENSP00000352900.5:n.442+323_442+341dup
ENST00000470566.1:n.367+323_367+341dup
ENST00000619224.1:c.73+323_73+341dup	ENSP00000482458.1:n.73+323_73+341dup
NM_001256570.1:c.73+323_73+341dup	NP_001243499.1:n.73+323_73+341dup
NM_001256571.1:c.73+323_73+341dup	NP_001243500.1:n.73+323_73+341dup
NM_006917.4:c.442+323_442+341dup	NP_008848.1:n.442+323_442+341dup
NM_006917.5:c.442+323_442+341dup MANE Select	NP_008848.1:n.442+323_442+341dup
NM_001256571.2:c.73+323_73+341dup	NP_001243500.1:n.73+323_73+341dup
NM_001256570.2:c.73+323_73+341dup	NP_001243499.1:n.73+323_73+341dup