Canonical Allele Identifier: CA375452108
Gene: RXRA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408188A>C , CM000671.2:g.134408188A>C GRCh38
NC_000009.11:g.137300034A>C , CM000671.1:g.137300034A>C GRCh37
NC_000009.10:g.136439855A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.319A>C MANE Select ENSP00000419692.1:p.Ile107Leu
ENST00000672570.1:c.238A>C ENSP00000500402.1:p.Ile80Leu
ENST00000356384.4:n.729A>C
ENST00000481739.1:c.319A>C ENSP00000419692.1:p.Ile107Leu
NM_001291920.1:c.238A>C NP_001278849.1:p.Ile80Leu
NM_001291921.1:c.28A>C NP_001278850.1:p.Ile10Leu
NM_002957.5:c.319A>C NP_002948.1:p.Ile107Leu
NM_002957.6:c.319A>C MANE Select NP_002948.1:p.Ile107Leu
NM_001291921.2:c.28A>C NP_001278850.1:p.Ile10Leu
NM_001291920.2:c.238A>C NP_001278849.1:p.Ile80Leu