Canonical Allele Identifier: CA467649042

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300135C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408289C>T , CM000671.2:g.134408289C>T	GRCh38
NC_000009.11:g.137300135C>T , CM000671.1:g.137300135C>T	GRCh37
NC_000009.10:g.136439956C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.420C>T MANE Select	ENSP00000419692.1:p.Asp140=
ENST00000672570.1:c.339C>T	ENSP00000500402.1:p.Asp113=
ENST00000356384.4:n.830C>T
ENST00000481739.1:c.420C>T	ENSP00000419692.1:p.Asp140=
NM_001291920.1:c.339C>T	NP_001278849.1:p.Asp113=
NM_001291921.1:c.129C>T	NP_001278850.1:p.Asp43=
NM_002957.5:c.420C>T	NP_002948.1:p.Asp140=
NM_002957.6:c.420C>T MANE Select	NP_002948.1:p.Asp140=
NM_001291921.2:c.129C>T	NP_001278850.1:p.Asp43=
NM_001291920.2:c.339C>T	NP_001278849.1:p.Asp113=