Canonical Allele Identifier: CA2692437077
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134408067-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408069del , CM000671.2:g.134408069del GRCh38
NC_000009.11:g.137299915del , CM000671.1:g.137299915del GRCh37
NC_000009.10:g.136439736del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.280-80del MANE Select ENSP00000419692.1:n.280-80del
ENST00000672570.1:c.199-80del ENSP00000500402.1:n.199-80del
ENST00000356384.4:n.690-80del
ENST00000481739.1:c.280-80del ENSP00000419692.1:n.280-80del
NM_001291920.1:c.199-80del NP_001278849.1:n.199-80del
NM_001291921.1:c.-12-80del NP_001278850.1:n.-12-80del
NM_002957.5:c.280-80del NP_002948.1:n.280-80del
NM_002957.6:c.280-80del MANE Select NP_002948.1:n.280-80del
NM_001291921.2:c.-12-80del NP_001278850.1:n.-12-80del
NM_001291920.2:c.199-80del NP_001278849.1:n.199-80del
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