Canonical Allele Identifier: CA1883176810
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408263A= , CM000671.2:g.134408263A= GRCh38
NC_000009.11:g.137300109A= , CM000671.1:g.137300109A= GRCh37
NC_000009.10:g.136439930A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.394A= MANE Select ENSP00000419692.1:p.Lys132=
ENST00000672570.1:c.313A= ENSP00000500402.1:p.Lys105=
ENST00000356384.4:n.804A=
ENST00000481739.1:c.394A= ENSP00000419692.1:p.Lys132=
NM_001291920.1:c.313A= NP_001278849.1:p.Lys105=
NM_001291921.1:c.103A= NP_001278850.1:p.Lys35=
NM_002957.5:c.394A= NP_002948.1:p.Lys132=
NM_002957.6:c.394A= MANE Select NP_002948.1:p.Lys132=
NM_001291921.2:c.103A= NP_001278850.1:p.Lys35=
NM_001291920.2:c.313A= NP_001278849.1:p.Lys105=