Canonical Allele Identifier: CA1883176658
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134407992G= , CM000671.2:g.134407992G= GRCh38
NC_000009.11:g.137299838G= , CM000671.1:g.137299838G= GRCh37
NC_000009.10:g.136439659G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.280-157G= MANE Select ENSP00000419692.1:n.280-157G=
ENST00000672570.1:c.199-157G= ENSP00000500402.1:n.199-157G=
ENST00000356384.4:n.690-157G=
ENST00000481739.1:c.280-157G= ENSP00000419692.1:n.280-157G=
NM_001291920.1:c.199-157G= NP_001278849.1:n.199-157G=
NM_001291921.1:c.-12-157G= NP_001278850.1:n.-12-157G=
NM_002957.5:c.280-157G= NP_002948.1:n.280-157G=
NM_002957.6:c.280-157G= MANE Select NP_002948.1:n.280-157G=
NM_001291921.2:c.-12-157G= NP_001278850.1:n.-12-157G=
NM_001291920.2:c.199-157G= NP_001278849.1:n.199-157G=