Canonical Allele Identifier: CA1883176822
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408295C= , CM000671.2:g.134408295C= GRCh38
NC_000009.11:g.137300141C= , CM000671.1:g.137300141C= GRCh37
NC_000009.10:g.136439962C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.426C= MANE Select ENSP00000419692.1:p.Ser142=
ENST00000672570.1:c.345C= ENSP00000500402.1:p.Ser115=
ENST00000356384.4:n.836C=
ENST00000481739.1:c.426C= ENSP00000419692.1:p.Ser142=
NM_001291920.1:c.345C= NP_001278849.1:p.Ser115=
NM_001291921.1:c.135C= NP_001278850.1:p.Ser45=
NM_002957.5:c.426C= NP_002948.1:p.Ser142=
NM_002957.6:c.426C= MANE Select NP_002948.1:p.Ser142=
NM_001291921.2:c.135C= NP_001278850.1:p.Ser45=
NM_001291920.2:c.345C= NP_001278849.1:p.Ser115=