Canonical Allele Identifier: CA1883186130

Gene: RXRA

Linked Data

• dbSNP Id: rs1831542226

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432123_134432124del , CM000671.2:g.134432123_134432124del	GRCh38
NC_000009.11:g.137323969_137323970del , CM000671.1:g.137323969_137323970del	GRCh37
NC_000009.10:g.136463790_136463791del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+127_1135+128del MANE Select	ENSP00000419692.1:n.1135+127_1135+128del
ENST00000672570.1:c.1054+127_1054+128del	ENSP00000500402.1:n.1054+127_1054+128del
ENST00000356384.4:n.1545+127_1545+128del
ENST00000481739.1:c.1135+127_1135+128del	ENSP00000419692.1:n.1135+127_1135+128del
NM_001291920.1:c.1054+127_1054+128del	NP_001278849.1:n.1054+127_1054+128del
NM_001291921.1:c.844+127_844+128del	NP_001278850.1:n.844+127_844+128del
NM_002957.5:c.1135+127_1135+128del	NP_002948.1:n.1135+127_1135+128del
NM_002957.6:c.1135+127_1135+128del MANE Select	NP_002948.1:n.1135+127_1135+128del
NM_001291921.2:c.844+127_844+128del	NP_001278850.1:n.844+127_844+128del
NM_001291920.2:c.1054+127_1054+128del	NP_001278849.1:n.1054+127_1054+128del