Canonical Allele Identifier: CA1883176808
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408255C= , CM000671.2:g.134408255C= GRCh38
NC_000009.11:g.137300101C= , CM000671.1:g.137300101C= GRCh37
NC_000009.10:g.136439922C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.386C= MANE Select ENSP00000419692.1:p.Ser129=
ENST00000672570.1:c.305C= ENSP00000500402.1:p.Ser102=
ENST00000356384.4:n.796C=
ENST00000481739.1:c.386C= ENSP00000419692.1:p.Ser129=
NM_001291920.1:c.305C= NP_001278849.1:p.Ser102=
NM_001291921.1:c.95C= NP_001278850.1:p.Ser32=
NM_002957.5:c.386C= NP_002948.1:p.Ser129=
NM_002957.6:c.386C= MANE Select NP_002948.1:p.Ser129=
NM_001291921.2:c.95C= NP_001278850.1:p.Ser32=
NM_001291920.2:c.305C= NP_001278849.1:p.Ser102=