Canonical Allele Identifier: CA2786204015
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408199_134408200dup , CM000671.2:g.134408199_134408200dup GRCh38
NC_000009.11:g.137300045_137300046dup , CM000671.1:g.137300045_137300046dup GRCh37
NC_000009.10:g.136439866_136439867dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.330_331dup MANE Select ENSP00000419692.1:p.Leu111ProfsTer?
ENST00000672570.1:c.249_250dup ENSP00000500402.1:p.Leu84ProfsTer?
ENST00000356384.4:n.740_741dup
ENST00000481739.1:c.330_331dup ENSP00000419692.1:p.Leu111ProfsTer?
NM_001291920.1:c.249_250dup NP_001278849.1:p.Leu84ProfsTer?
NM_001291921.1:c.39_40dup NP_001278850.1:p.Leu14ProfsTer?
NM_002957.5:c.330_331dup NP_002948.1:p.Leu111ProfsTer?
NM_002957.6:c.330_331dup MANE Select NP_002948.1:p.Leu111ProfsTer?
NM_001291921.2:c.39_40dup NP_001278850.1:p.Leu14ProfsTer?
NM_001291920.2:c.249_250dup NP_001278849.1:p.Leu84ProfsTer?