Canonical Allele Identifier: CA1883176807
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408249T= , CM000671.2:g.134408249T= GRCh38
NC_000009.11:g.137300095T= , CM000671.1:g.137300095T= GRCh37
NC_000009.10:g.136439916T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.380T= MANE Select ENSP00000419692.1:p.Met127=
ENST00000672570.1:c.299T= ENSP00000500402.1:p.Met100=
ENST00000356384.4:n.790T=
ENST00000481739.1:c.380T= ENSP00000419692.1:p.Met127=
NM_001291920.1:c.299T= NP_001278849.1:p.Met100=
NM_001291921.1:c.89T= NP_001278850.1:p.Met30=
NM_002957.5:c.380T= NP_002948.1:p.Met127=
NM_002957.6:c.380T= MANE Select NP_002948.1:p.Met127=
NM_001291921.2:c.89T= NP_001278850.1:p.Met30=
NM_001291920.2:c.299T= NP_001278849.1:p.Met100=