Canonical Allele Identifier: CA5317691

Gene: RXRA

Linked Data

• dbSNP Id: rs1805340
• ExAC: 9:137299984 G / GC
• gnomAD v2: 9-137299984-G-GC
• gnomAD v3: 9-134408138-G-GC
• gnomAD v4: 9-134408138-G-GC
• COSMIC: COSN1374975 ; COSM5499059
• MyVariant Identifiers: chr9:g.137299985_137299986insC (hg19) ; chr9:g.137299984_137299985insC (hg19) ; chr9:g.134408139_134408140insC (hg38) ; chr9:g.134408138_134408139insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408146dup , CM000671.2:g.134408146dup	GRCh38
NC_000009.11:g.137299992dup , CM000671.1:g.137299992dup	GRCh37
NC_000009.10:g.136439813dup	NCBI36

Transcript Alleles

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