Canonical Allele Identifier: CA527078961

Gene: RXRG

Linked Data

• dbSNP Id: rs1225418681
• gnomAD v2: 1-165409192-GAGA-G
• gnomAD v3: 1-165439955-GAGA-G
• gnomAD v4: 1-165439955-GAGA-G
• MyVariant Identifiers: chr1:g.165409193_165409195del (hg19) ; chr1:g.165439956_165439958del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439962_165439964del , CM000663.2:g.165439962_165439964del	GRCh38
NC_000001.10:g.165409199_165409201del , CM000663.1:g.165409199_165409201del	GRCh37
NC_000001.9:g.163675823_163675825del	NCBI36
NG_029517.1:g.10398_10400del
NG_029517.2:g.10398_10400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4887_49+4889del MANE Select	ENSP00000352900.5:n.49+4887_49+4889del
ENST00000359842.9:c.49+4887_49+4889del	ENSP00000352900.5:n.49+4887_49+4889del
ENST00000465764.1:n.329-2757_329-2755del
ENST00000619224.1:c.-379+4887_-379+4889del	ENSP00000482458.1:n.-379+4887_-379+4889del
NM_001256570.1:c.-379+4887_-379+4889del	NP_001243499.1:n.-379+4887_-379+4889del
NM_006917.4:c.49+4887_49+4889del	NP_008848.1:n.49+4887_49+4889del
NR_033824.1:n.512-2757_512-2755del
NM_006917.5:c.49+4887_49+4889del MANE Select	NP_008848.1:n.49+4887_49+4889del
NR_033824.2:n.283-2757_283-2755del
NM_001256570.2:c.-379+4887_-379+4889del	NP_001243499.1:n.-379+4887_-379+4889del