Canonical Allele Identifier: CA375452176

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408201-T-G
• MyVariant Identifiers: chr9:g.137300047T>G (hg19) ; chr9:g.134408201T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408201T>G , CM000671.2:g.134408201T>G	GRCh38
NC_000009.11:g.137300047T>G , CM000671.1:g.137300047T>G	GRCh37
NC_000009.10:g.136439868T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.332T>G MANE Select	ENSP00000419692.1:p.Leu111Arg
ENST00000672570.1:c.251T>G	ENSP00000500402.1:p.Leu84Arg
ENST00000356384.4:n.742T>G
ENST00000481739.1:c.332T>G	ENSP00000419692.1:p.Leu111Arg
NM_001291920.1:c.251T>G	NP_001278849.1:p.Leu84Arg
NM_001291921.1:c.41T>G	NP_001278850.1:p.Leu14Arg
NM_002957.5:c.332T>G	NP_002948.1:p.Leu111Arg
NM_002957.6:c.332T>G MANE Select	NP_002948.1:p.Leu111Arg
NM_001291921.2:c.41T>G	NP_001278850.1:p.Leu14Arg
NM_001291920.2:c.251T>G	NP_001278849.1:p.Leu84Arg