Canonical Allele Identifier: CA467649025

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300132G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408286G>C , CM000671.2:g.134408286G>C	GRCh38
NC_000009.11:g.137300132G>C , CM000671.1:g.137300132G>C	GRCh37
NC_000009.10:g.136439953G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.417G>C MANE Select	ENSP00000419692.1:p.Gly139=
ENST00000672570.1:c.336G>C	ENSP00000500402.1:p.Gly112=
ENST00000356384.4:n.827G>C
ENST00000481739.1:c.417G>C	ENSP00000419692.1:p.Gly139=
NM_001291920.1:c.336G>C	NP_001278849.1:p.Gly112=
NM_001291921.1:c.126G>C	NP_001278850.1:p.Gly42=
NM_002957.5:c.417G>C	NP_002948.1:p.Gly139=
NM_002957.6:c.417G>C MANE Select	NP_002948.1:p.Gly139=
NM_001291921.2:c.126G>C	NP_001278850.1:p.Gly42=
NM_001291920.2:c.336G>C	NP_001278849.1:p.Gly112=