Canonical Allele Identifier: CA1883176787
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408201T= , CM000671.2:g.134408201T= GRCh38
NC_000009.11:g.137300047T= , CM000671.1:g.137300047T= GRCh37
NC_000009.10:g.136439868T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.332T= MANE Select ENSP00000419692.1:p.Leu111=
ENST00000672570.1:c.251T= ENSP00000500402.1:p.Leu84=
ENST00000356384.4:n.742T=
ENST00000481739.1:c.332T= ENSP00000419692.1:p.Leu111=
NM_001291920.1:c.251T= NP_001278849.1:p.Leu84=
NM_001291921.1:c.41T= NP_001278850.1:p.Leu14=
NM_002957.5:c.332T= NP_002948.1:p.Leu111=
NM_002957.6:c.332T= MANE Select NP_002948.1:p.Leu111=
NM_001291921.2:c.41T= NP_001278850.1:p.Leu14=
NM_001291920.2:c.251T= NP_001278849.1:p.Leu84=