Canonical Allele Identifier: CA527077823

Gene: RXRG

Linked Data

• dbSNP Id: rs1220419382
• gnomAD v2: 1-165389279-A-ACAGAGC
• gnomAD v4: 1-165420042-A-ACAGAGC
• MyVariant Identifiers: chr1:g.165389279_165389280insCAGAGC (hg19) ; chr1:g.165420042_165420043insCAGAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420048_165420053dup , CM000663.2:g.165420048_165420053dup	GRCh38
NC_000001.10:g.165389285_165389290dup , CM000663.1:g.165389285_165389290dup	GRCh37
NC_000001.9:g.163655909_163655914dup	NCBI36
NG_029517.1:g.30308_30313dup
NG_029517.2:g.30308_30313dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-34_298-29dup MANE Select	ENSP00000352900.5:n.298-34_298-29dup
ENST00000359842.9:c.298-34_298-29dup	ENSP00000352900.5:n.298-34_298-29dup
ENST00000470566.1:n.223-34_223-29dup
ENST00000619224.1:c.-72-34_-72-29dup	ENSP00000482458.1:n.-72-34_-72-29dup
NM_001256570.1:c.-72-34_-72-29dup	NP_001243499.1:n.-72-34_-72-29dup
NM_001256571.1:c.-72-34_-72-29dup	NP_001243500.1:n.-72-34_-72-29dup
NM_006917.4:c.298-34_298-29dup	NP_008848.1:n.298-34_298-29dup
NM_006917.5:c.298-34_298-29dup MANE Select	NP_008848.1:n.298-34_298-29dup
NM_001256571.2:c.-72-34_-72-29dup	NP_001243500.1:n.-72-34_-72-29dup
NM_001256570.2:c.-72-34_-72-29dup	NP_001243499.1:n.-72-34_-72-29dup