Canonical Allele Identifier: CA467648856

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300099T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408253T>C , CM000671.2:g.134408253T>C	GRCh38
NC_000009.11:g.137300099T>C , CM000671.1:g.137300099T>C	GRCh37
NC_000009.10:g.136439920T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.384T>C MANE Select	ENSP00000419692.1:p.Ala128=
ENST00000672570.1:c.303T>C	ENSP00000500402.1:p.Ala101=
ENST00000356384.4:n.794T>C
ENST00000481739.1:c.384T>C	ENSP00000419692.1:p.Ala128=
NM_001291920.1:c.303T>C	NP_001278849.1:p.Ala101=
NM_001291921.1:c.93T>C	NP_001278850.1:p.Ala31=
NM_002957.5:c.384T>C	NP_002948.1:p.Ala128=
NM_002957.6:c.384T>C MANE Select	NP_002948.1:p.Ala128=
NM_001291921.2:c.93T>C	NP_001278850.1:p.Ala31=
NM_001291920.2:c.303T>C	NP_001278849.1:p.Ala101=