Canonical Allele Identifier: CA1129841868
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1831120667

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409904_134409921del , CM000671.2:g.134409904_134409921del GRCh38
NC_000009.11:g.137301750_137301767del , CM000671.1:g.137301750_137301767del GRCh37
NC_000009.10:g.136441571_136441588del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.610+785_610+802del MANE Select ENSP00000419692.1:n.610+785_610+802del
ENST00000672570.1:c.529+785_529+802del ENSP00000500402.1:n.529+785_529+802del
ENST00000356384.4:n.1020+785_1020+802del
ENST00000481739.1:c.610+785_610+802del ENSP00000419692.1:n.610+785_610+802del
NM_001291920.1:c.529+785_529+802del NP_001278849.1:n.529+785_529+802del
NM_001291921.1:c.319+785_319+802del NP_001278850.1:n.319+785_319+802del
NM_002957.5:c.610+785_610+802del NP_002948.1:n.610+785_610+802del
NM_002957.6:c.610+785_610+802del MANE Select NP_002948.1:n.610+785_610+802del
NM_001291921.2:c.319+785_319+802del NP_001278850.1:n.319+785_319+802del
NM_001291920.2:c.529+785_529+802del NP_001278849.1:n.529+785_529+802del