Canonical Allele Identifier: CA1883176632
Gene: RXRA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134407944A= , CM000671.2:g.134407944A= GRCh38
NC_000009.11:g.137299790A= , CM000671.1:g.137299790A= GRCh37
NC_000009.10:g.136439611A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.280-205A= MANE Select ENSP00000419692.1:n.280-205A=
ENST00000672570.1:c.199-205A= ENSP00000500402.1:n.199-205A=
ENST00000356384.4:n.690-205A=
ENST00000481739.1:c.280-205A= ENSP00000419692.1:n.280-205A=
NM_001291920.1:c.199-205A= NP_001278849.1:n.199-205A=
NM_001291921.1:c.-12-205A= NP_001278850.1:n.-12-205A=
NM_002957.5:c.280-205A= NP_002948.1:n.280-205A=
NM_002957.6:c.280-205A= MANE Select NP_002948.1:n.280-205A=
NM_001291921.2:c.-12-205A= NP_001278850.1:n.-12-205A=
NM_001291920.2:c.199-205A= NP_001278849.1:n.199-205A=
Search 100 bp 5'
Search 100 bp 3'