Canonical Allele Identifier: CA467649029

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300132G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408286G>A , CM000671.2:g.134408286G>A	GRCh38
NC_000009.11:g.137300132G>A , CM000671.1:g.137300132G>A	GRCh37
NC_000009.10:g.136439953G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.417G>A MANE Select	ENSP00000419692.1:p.Gly139=
ENST00000672570.1:c.336G>A	ENSP00000500402.1:p.Gly112=
ENST00000356384.4:n.827G>A
ENST00000481739.1:c.417G>A	ENSP00000419692.1:p.Gly139=
NM_001291920.1:c.336G>A	NP_001278849.1:p.Gly112=
NM_001291921.1:c.126G>A	NP_001278850.1:p.Gly42=
NM_002957.5:c.417G>A	NP_002948.1:p.Gly139=
NM_002957.6:c.417G>A MANE Select	NP_002948.1:p.Gly139=
NM_001291921.2:c.126G>A	NP_001278850.1:p.Gly42=
NM_001291920.2:c.336G>A	NP_001278849.1:p.Gly112=