Canonical Allele Identifier: CA860856111

Gene: RXRA

Linked Data

• dbSNP Id: rs1330472340
• gnomAD v4: 9-134408052-TGGG-T
• MyVariant Identifiers: chr9:g.137299899_137299901del (hg19) ; chr9:g.134408053_134408055del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408055_134408057del , CM000671.2:g.134408055_134408057del	GRCh38
NC_000009.11:g.137299901_137299903del , CM000671.1:g.137299901_137299903del	GRCh37
NC_000009.10:g.136439722_136439724del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.280-94_280-92del MANE Select	ENSP00000419692.1:n.280-94_280-92del
ENST00000672570.1:c.199-94_199-92del	ENSP00000500402.1:n.199-94_199-92del
ENST00000356384.4:n.690-94_690-92del
ENST00000481739.1:c.280-94_280-92del	ENSP00000419692.1:n.280-94_280-92del
NM_001291920.1:c.199-94_199-92del	NP_001278849.1:n.199-94_199-92del
NM_001291921.1:c.-12-94_-12-92del	NP_001278850.1:n.-12-94_-12-92del
NM_002957.5:c.280-94_280-92del	NP_002948.1:n.280-94_280-92del
NM_002957.6:c.280-94_280-92del MANE Select	NP_002948.1:n.280-94_280-92del
NM_001291921.2:c.-12-94_-12-92del	NP_001278850.1:n.-12-94_-12-92del
NM_001291920.2:c.199-94_199-92del	NP_001278849.1:n.199-94_199-92del