Canonical Allele Identifier: CA527078953

Gene: RXRG

Linked Data

• dbSNP Id: rs1457402724
• gnomAD v2: 1-165408881-TCCCCACTGAGGAAGCCAGAA-T
• gnomAD v3: 1-165439644-TCCCCACTGAGGAAGCCAGAA-T
• gnomAD v4: 1-165439644-TCCCCACTGAGGAAGCCAGAA-T
• MyVariant Identifiers: chr1:g.165408882_165408901del (hg19) ; chr1:g.165439645_165439664del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439645_165439664del , CM000663.2:g.165439645_165439664del	GRCh38
NC_000001.10:g.165408882_165408901del , CM000663.1:g.165408882_165408901del	GRCh37
NC_000001.9:g.163675506_163675525del	NCBI36
NG_029517.1:g.10692_10711del
NG_029517.2:g.10692_10711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5181_49+5200del MANE Select	ENSP00000352900.5:n.49+5181_49+5200del
ENST00000359842.9:c.49+5181_49+5200del	ENSP00000352900.5:n.49+5181_49+5200del
ENST00000465764.1:n.329-2463_329-2444del
ENST00000619224.1:c.-379+5181_-379+5200del	ENSP00000482458.1:n.-379+5181_-379+5200del
NM_001256570.1:c.-379+5181_-379+5200del	NP_001243499.1:n.-379+5181_-379+5200del
NM_006917.4:c.49+5181_49+5200del	NP_008848.1:n.49+5181_49+5200del
NR_033824.1:n.512-2463_512-2444del
NM_006917.5:c.49+5181_49+5200del MANE Select	NP_008848.1:n.49+5181_49+5200del
NR_033824.2:n.283-2463_283-2444del
NM_001256570.2:c.-379+5181_-379+5200del	NP_001243499.1:n.-379+5181_-379+5200del