Canonical Allele Identifier: CA201046722
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134416616A>C , CM000671.2:g.134416616A>C GRCh38
NC_000009.11:g.137308462A>C , CM000671.1:g.137308462A>C GRCh37
NC_000009.10:g.136448283A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.611-542A>C MANE Select ENSP00000419692.1:n.611-542A>C
ENST00000672570.1:c.530-542A>C ENSP00000500402.1:n.530-542A>C
ENST00000356384.4:n.1021-542A>C
ENST00000481739.1:c.611-542A>C ENSP00000419692.1:n.611-542A>C
NM_001291920.1:c.530-542A>C NP_001278849.1:n.530-542A>C
NM_001291921.1:c.320-542A>C NP_001278850.1:n.320-542A>C
NM_002957.5:c.611-542A>C NP_002948.1:n.611-542A>C
NM_002957.6:c.611-542A>C MANE Select NP_002948.1:n.611-542A>C
NM_001291921.2:c.320-542A>C NP_001278850.1:n.320-542A>C
NM_001291920.2:c.530-542A>C NP_001278849.1:n.530-542A>C
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