Canonical Allele Identifier: CA1883177580
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409739T= , CM000671.2:g.134409739T= GRCh38
NC_000009.11:g.137301585T= , CM000671.1:g.137301585T= GRCh37
NC_000009.10:g.136441406T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.610+620T= MANE Select ENSP00000419692.1:n.610+620T=
ENST00000672570.1:c.529+620T= ENSP00000500402.1:n.529+620T=
ENST00000356384.4:n.1020+620T=
ENST00000481739.1:c.610+620T= ENSP00000419692.1:n.610+620T=
NM_001291920.1:c.529+620T= NP_001278849.1:n.529+620T=
NM_001291921.1:c.319+620T= NP_001278850.1:n.319+620T=
NM_002957.5:c.610+620T= NP_002948.1:n.610+620T=
NM_002957.6:c.610+620T= MANE Select NP_002948.1:n.610+620T=
NM_001291921.2:c.319+620T= NP_001278850.1:n.319+620T=
NM_001291920.2:c.529+620T= NP_001278849.1:n.529+620T=
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