Canonical Allele Identifier: CA1883186126

Gene: RXRA

Linked Data

• dbSNP Id: rs1831542089
• gnomAD v4: 9-134432115-CTTGAGCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432116_134432122del , CM000671.2:g.134432116_134432122del	GRCh38
NC_000009.11:g.137323962_137323968del , CM000671.1:g.137323962_137323968del	GRCh37
NC_000009.10:g.136463783_136463789del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+120_1135+126del MANE Select	ENSP00000419692.1:n.1135+120_1135+126del
ENST00000672570.1:c.1054+120_1054+126del	ENSP00000500402.1:n.1054+120_1054+126del
ENST00000356384.4:n.1545+120_1545+126del
ENST00000481739.1:c.1135+120_1135+126del	ENSP00000419692.1:n.1135+120_1135+126del
NM_001291920.1:c.1054+120_1054+126del	NP_001278849.1:n.1054+120_1054+126del
NM_001291921.1:c.844+120_844+126del	NP_001278850.1:n.844+120_844+126del
NM_002957.5:c.1135+120_1135+126del	NP_002948.1:n.1135+120_1135+126del
NM_002957.6:c.1135+120_1135+126del MANE Select	NP_002948.1:n.1135+120_1135+126del
NM_001291921.2:c.844+120_844+126del	NP_001278850.1:n.844+120_844+126del
NM_001291920.2:c.1054+120_1054+126del	NP_001278849.1:n.1054+120_1054+126del