Canonical Allele Identifier: CA1883176820
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408291G= , CM000671.2:g.134408291G= GRCh38
NC_000009.11:g.137300137G= , CM000671.1:g.137300137G= GRCh37
NC_000009.10:g.136439958G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.422G= MANE Select ENSP00000419692.1:p.Arg141=
ENST00000672570.1:c.341G= ENSP00000500402.1:p.Arg114=
ENST00000356384.4:n.832G=
ENST00000481739.1:c.422G= ENSP00000419692.1:p.Arg141=
NM_001291920.1:c.341G= NP_001278849.1:p.Arg114=
NM_001291921.1:c.131G= NP_001278850.1:p.Arg44=
NM_002957.5:c.422G= NP_002948.1:p.Arg141=
NM_002957.6:c.422G= MANE Select NP_002948.1:p.Arg141=
NM_001291921.2:c.131G= NP_001278850.1:p.Arg44=
NM_001291920.2:c.341G= NP_001278849.1:p.Arg114=