Canonical Allele Identifier: CA467649087

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300144A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408298A>C , CM000671.2:g.134408298A>C	GRCh38
NC_000009.11:g.137300144A>C , CM000671.1:g.137300144A>C	GRCh37
NC_000009.10:g.136439965A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.429A>C MANE Select	ENSP00000419692.1:p.Ser143=
ENST00000672570.1:c.348A>C	ENSP00000500402.1:p.Ser116=
ENST00000356384.4:n.839A>C
ENST00000481739.1:c.429A>C	ENSP00000419692.1:p.Ser143=
NM_001291920.1:c.348A>C	NP_001278849.1:p.Ser116=
NM_001291921.1:c.138A>C	NP_001278850.1:p.Ser46=
NM_002957.5:c.429A>C	NP_002948.1:p.Ser143=
NM_002957.6:c.429A>C MANE Select	NP_002948.1:p.Ser143=
NM_001291921.2:c.138A>C	NP_001278850.1:p.Ser46=
NM_001291920.2:c.348A>C	NP_001278849.1:p.Ser116=