Canonical Allele Identifier: CA1883176814
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408275G= , CM000671.2:g.134408275G= GRCh38
NC_000009.11:g.137300121G= , CM000671.1:g.137300121G= GRCh37
NC_000009.10:g.136439942G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.406G= MANE Select ENSP00000419692.1:p.Ala136=
ENST00000672570.1:c.325G= ENSP00000500402.1:p.Ala109=
ENST00000356384.4:n.816G=
ENST00000481739.1:c.406G= ENSP00000419692.1:p.Ala136=
NM_001291920.1:c.325G= NP_001278849.1:p.Ala109=
NM_001291921.1:c.115G= NP_001278850.1:p.Ala39=
NM_002957.5:c.406G= NP_002948.1:p.Ala136=
NM_002957.6:c.406G= MANE Select NP_002948.1:p.Ala136=
NM_001291921.2:c.115G= NP_001278850.1:p.Ala39=
NM_001291920.2:c.325G= NP_001278849.1:p.Ala109=