Canonical Allele Identifier: CA860856122
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1398116098
MyVariant Identifiers: chr9:g.137299913_137299914insC (hg19) chr9:g.134408067_134408068insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408069dup , CM000671.2:g.134408069dup GRCh38
NC_000009.11:g.137299915dup , CM000671.1:g.137299915dup GRCh37
NC_000009.10:g.136439736dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.280-80dup MANE Select ENSP00000419692.1:n.280-80dup
ENST00000672570.1:c.199-80dup ENSP00000500402.1:n.199-80dup
ENST00000356384.4:n.690-80dup
ENST00000481739.1:c.280-80dup ENSP00000419692.1:n.280-80dup
NM_001291920.1:c.199-80dup NP_001278849.1:n.199-80dup
NM_001291921.1:c.-12-80dup NP_001278850.1:n.-12-80dup
NM_002957.5:c.280-80dup NP_002948.1:n.280-80dup
NM_002957.6:c.280-80dup MANE Select NP_002948.1:n.280-80dup
NM_001291921.2:c.-12-80dup NP_001278850.1:n.-12-80dup
NM_001291920.2:c.199-80dup NP_001278849.1:n.199-80dup
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