Canonical Allele Identifier: CA1883171830
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134398793G= , CM000671.2:g.134398793G= GRCh38
NC_000009.11:g.137290639G= , CM000671.1:g.137290639G= GRCh37
NC_000009.10:g.136430460G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-2839G= MANE Select ENSP00000419692.1:n.29-2839G=
ENST00000649020.1:c.119-2839G= ENSP00000497073.1:n.119-2839G=
ENST00000672570.1:c.-53-2839G= ENSP00000500402.1:n.-53-2839G=
ENST00000356384.4:n.294-2603G=
ENST00000481739.1:c.29-2839G= ENSP00000419692.1:n.29-2839G=
ENST00000484822.1:n.453-2839G=
NM_001291920.1:c.-53-2839G= NP_001278849.1:n.-53-2839G=
NM_002957.5:c.29-2839G= NP_002948.1:n.29-2839G=
NM_002957.6:c.29-2839G= MANE Select NP_002948.1:n.29-2839G=
NM_001291920.2:c.-53-2839G= NP_001278849.1:n.-53-2839G=
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