Canonical Allele Identifier: CA375452380

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300077C>A (hg19) ; chr9:g.134408231C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408231C>A , CM000671.2:g.134408231C>A	GRCh38
NC_000009.11:g.137300077C>A , CM000671.1:g.137300077C>A	GRCh37
NC_000009.10:g.136439898C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.362C>A MANE Select	ENSP00000419692.1:p.Ala121Asp
ENST00000672570.1:c.281C>A	ENSP00000500402.1:p.Ala94Asp
ENST00000356384.4:n.772C>A
ENST00000481739.1:c.362C>A	ENSP00000419692.1:p.Ala121Asp
NM_001291920.1:c.281C>A	NP_001278849.1:p.Ala94Asp
NM_001291921.1:c.71C>A	NP_001278850.1:p.Ala24Asp
NM_002957.5:c.362C>A	NP_002948.1:p.Ala121Asp
NM_002957.6:c.362C>A MANE Select	NP_002948.1:p.Ala121Asp
NM_001291921.2:c.71C>A	NP_001278850.1:p.Ala24Asp
NM_001291920.2:c.281C>A	NP_001278849.1:p.Ala94Asp