Canonical Allele Identifier: CA1883184387
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134429009G= , CM000671.2:g.134429009G= GRCh38
NC_000009.11:g.137320855G= , CM000671.1:g.137320855G= GRCh37
NC_000009.10:g.136460676G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.911-99G= MANE Select ENSP00000419692.1:n.911-99G=
ENST00000672570.1:c.830-99G= ENSP00000500402.1:n.830-99G=
ENST00000356384.4:n.1321-99G=
ENST00000481739.1:c.911-99G= ENSP00000419692.1:n.911-99G=
NM_001291920.1:c.830-99G= NP_001278849.1:n.830-99G=
NM_001291921.1:c.620-99G= NP_001278850.1:n.620-99G=
NM_002957.5:c.911-99G= NP_002948.1:n.911-99G=
NM_002957.6:c.911-99G= MANE Select NP_002948.1:n.911-99G=
NM_001291921.2:c.620-99G= NP_001278850.1:n.620-99G=
NM_001291920.2:c.830-99G= NP_001278849.1:n.830-99G=