Canonical Allele Identifier: CA375452142

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408194-C-G
• MyVariant Identifiers: chr9:g.137300040C>G (hg19) ; chr9:g.134408194C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408194C>G , CM000671.2:g.134408194C>G	GRCh38
NC_000009.11:g.137300040C>G , CM000671.1:g.137300040C>G	GRCh37
NC_000009.10:g.136439861C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.325C>G MANE Select	ENSP00000419692.1:p.Pro109Ala
ENST00000672570.1:c.244C>G	ENSP00000500402.1:p.Pro82Ala
ENST00000356384.4:n.735C>G
ENST00000481739.1:c.325C>G	ENSP00000419692.1:p.Pro109Ala
NM_001291920.1:c.244C>G	NP_001278849.1:p.Pro82Ala
NM_001291921.1:c.34C>G	NP_001278850.1:p.Pro12Ala
NM_002957.5:c.325C>G	NP_002948.1:p.Pro109Ala
NM_002957.6:c.325C>G MANE Select	NP_002948.1:p.Pro109Ala
NM_001291921.2:c.34C>G	NP_001278850.1:p.Pro12Ala
NM_001291920.2:c.244C>G	NP_001278849.1:p.Pro82Ala