Canonical Allele Identifier: CA1883176798
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408228C= , CM000671.2:g.134408228C= GRCh38
NC_000009.11:g.137300074C= , CM000671.1:g.137300074C= GRCh37
NC_000009.10:g.136439895C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.359C= MANE Select ENSP00000419692.1:p.Pro120=
ENST00000672570.1:c.278C= ENSP00000500402.1:p.Pro93=
ENST00000356384.4:n.769C=
ENST00000481739.1:c.359C= ENSP00000419692.1:p.Pro120=
NM_001291920.1:c.278C= NP_001278849.1:p.Pro93=
NM_001291921.1:c.68C= NP_001278850.1:p.Pro23=
NM_002957.5:c.359C= NP_002948.1:p.Pro120=
NM_002957.6:c.359C= MANE Select NP_002948.1:p.Pro120=
NM_001291921.2:c.68C= NP_001278850.1:p.Pro23=
NM_001291920.2:c.278C= NP_001278849.1:p.Pro93=