Canonical Allele Identifier: CA375452667

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300124A>T (hg19) ; chr9:g.134408278A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408278A>T , CM000671.2:g.134408278A>T	GRCh38
NC_000009.11:g.137300124A>T , CM000671.1:g.137300124A>T	GRCh37
NC_000009.10:g.136439945A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.409A>T MANE Select	ENSP00000419692.1:p.Ile137Phe
ENST00000672570.1:c.328A>T	ENSP00000500402.1:p.Ile110Phe
ENST00000356384.4:n.819A>T
ENST00000481739.1:c.409A>T	ENSP00000419692.1:p.Ile137Phe
NM_001291920.1:c.328A>T	NP_001278849.1:p.Ile110Phe
NM_001291921.1:c.118A>T	NP_001278850.1:p.Ile40Phe
NM_002957.5:c.409A>T	NP_002948.1:p.Ile137Phe
NM_002957.6:c.409A>T MANE Select	NP_002948.1:p.Ile137Phe
NM_001291921.2:c.118A>T	NP_001278850.1:p.Ile40Phe
NM_001291920.2:c.328A>T	NP_001278849.1:p.Ile110Phe