Canonical Allele Identifier: CA1883186142

Gene: RXRA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432135_134432136delinsCT , CM000671.2:g.134432135_134432136delinsCT	GRCh38
NC_000009.11:g.137323981_137323982delinsCT , CM000671.1:g.137323981_137323982delinsCT	GRCh37
NC_000009.10:g.136463802_136463803delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+139_1135+140delinsCT MANE Select	ENSP00000419692.1:n.1135+139_1135+140deli...
ENST00000672570.1:c.1054+139_1054+140delinsCT	ENSP00000500402.1:n.1054+139_1054+140deli...
ENST00000356384.4:n.1545+139_1545+140delinsCT
ENST00000481739.1:c.1135+139_1135+140delinsCT	ENSP00000419692.1:n.1135+139_1135+140deli...
NM_001291920.1:c.1054+139_1054+140delinsCT	NP_001278849.1:n.1054+139_1054+140delinsC...
NM_001291921.1:c.844+139_844+140delinsCT	NP_001278850.1:n.844+139_844+140delinsCT
NM_002957.5:c.1135+139_1135+140delinsCT	NP_002948.1:n.1135+139_1135+140delinsCT
NM_002957.6:c.1135+139_1135+140delinsCT MANE Select	NP_002948.1:n.1135+139_1135+140delinsCT
NM_001291921.2:c.844+139_844+140delinsCT	NP_001278850.1:n.844+139_844+140delinsCT
NM_001291920.2:c.1054+139_1054+140delinsCT	NP_001278849.1:n.1054+139_1054+140delinsC...