Canonical Allele Identifier: CA1883171835
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134398803C= , CM000671.2:g.134398803C= GRCh38
NC_000009.11:g.137290649C= , CM000671.1:g.137290649C= GRCh37
NC_000009.10:g.136430470C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-2829C= MANE Select ENSP00000419692.1:n.29-2829C=
ENST00000649020.1:c.119-2829C= ENSP00000497073.1:n.119-2829C=
ENST00000672570.1:c.-53-2829C= ENSP00000500402.1:n.-53-2829C=
ENST00000356384.4:n.294-2593C=
ENST00000481739.1:c.29-2829C= ENSP00000419692.1:n.29-2829C=
ENST00000484822.1:n.453-2829C=
NM_001291920.1:c.-53-2829C= NP_001278849.1:n.-53-2829C=
NM_002957.5:c.29-2829C= NP_002948.1:n.29-2829C=
NM_002957.6:c.29-2829C= MANE Select NP_002948.1:n.29-2829C=
NM_001291920.2:c.-53-2829C= NP_001278849.1:n.-53-2829C=
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