Canonical Allele Identifier: CA1883186120
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134432112C= , CM000671.2:g.134432112C= GRCh38
NC_000009.11:g.137323958C= , CM000671.1:g.137323958C= GRCh37
NC_000009.10:g.136463779C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.1135+116C= MANE Select ENSP00000419692.1:n.1135+116C=
ENST00000672570.1:c.1054+116C= ENSP00000500402.1:n.1054+116C=
ENST00000356384.4:n.1545+116C=
ENST00000481739.1:c.1135+116C= ENSP00000419692.1:n.1135+116C=
NM_001291920.1:c.1054+116C= NP_001278849.1:n.1054+116C=
NM_001291921.1:c.844+116C= NP_001278850.1:n.844+116C=
NM_002957.5:c.1135+116C= NP_002948.1:n.1135+116C=
NM_002957.6:c.1135+116C= MANE Select NP_002948.1:n.1135+116C=
NM_001291921.2:c.844+116C= NP_001278850.1:n.844+116C=
NM_001291920.2:c.1054+116C= NP_001278849.1:n.1054+116C=