Canonical Allele Identifier: CA1883191170
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134433976T>A , CM000671.2:g.134433976T>A GRCh38
NC_000009.11:g.137325822T>A , CM000671.1:g.137325822T>A GRCh37
NC_000009.10:g.136465643T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.1136-126T>A MANE Select ENSP00000419692.1:n.1136-126T>A
ENST00000672570.1:c.1055-126T>A ENSP00000500402.1:n.1055-126T>A
ENST00000356384.4:n.1546-126T>A
ENST00000481739.1:c.1136-126T>A ENSP00000419692.1:n.1136-126T>A
NM_001291920.1:c.1055-126T>A NP_001278849.1:n.1055-126T>A
NM_001291921.1:c.845-126T>A NP_001278850.1:n.845-126T>A
NM_002957.5:c.1136-126T>A NP_002948.1:n.1136-126T>A
NM_002957.6:c.1136-126T>A MANE Select NP_002948.1:n.1136-126T>A
NM_001291921.2:c.845-126T>A NP_001278850.1:n.845-126T>A
NM_001291920.2:c.1055-126T>A NP_001278849.1:n.1055-126T>A