Canonical Allele Identifier: CA2692437093
Gene: RXRA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408077_134408095del , CM000671.2:g.134408077_134408095del GRCh38
NC_000009.11:g.137299923_137299941del , CM000671.1:g.137299923_137299941del GRCh37
NC_000009.10:g.136439744_136439762del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.280-72_280-54del MANE Select ENSP00000419692.1:n.280-72_280-54del
ENST00000672570.1:c.199-72_199-54del ENSP00000500402.1:n.199-72_199-54del
ENST00000356384.4:n.690-72_690-54del
ENST00000481739.1:c.280-72_280-54del ENSP00000419692.1:n.280-72_280-54del
NM_001291920.1:c.199-72_199-54del NP_001278849.1:n.199-72_199-54del
NM_001291921.1:c.-12-72_-12-54del NP_001278850.1:n.-12-72_-12-54del
NM_002957.5:c.280-72_280-54del NP_002948.1:n.280-72_280-54del
NM_002957.6:c.280-72_280-54del MANE Select NP_002948.1:n.280-72_280-54del
NM_001291921.2:c.-12-72_-12-54del NP_001278850.1:n.-12-72_-12-54del
NM_001291920.2:c.199-72_199-54del NP_001278849.1:n.199-72_199-54del