Canonical Allele Identifier: CA467647812

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300006T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408160T>G , CM000671.2:g.134408160T>G	GRCh38
NC_000009.11:g.137300006T>G , CM000671.1:g.137300006T>G	GRCh37
NC_000009.10:g.136439827T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.291T>G MANE Select	ENSP00000419692.1:p.Pro97=
ENST00000672570.1:c.210T>G	ENSP00000500402.1:p.Pro70=
ENST00000356384.4:n.701T>G
ENST00000481739.1:c.291T>G	ENSP00000419692.1:p.Pro97=
NM_001291920.1:c.210T>G	NP_001278849.1:p.Pro70=
NM_001291921.1:c.-1T>G	NP_001278850.1:n.-1T>G
NM_002957.5:c.291T>G	NP_002948.1:p.Pro97=
NM_002957.6:c.291T>G MANE Select	NP_002948.1:p.Pro97=
NM_001291921.2:c.-1T>G	NP_001278850.1:n.-1T>G
NM_001291920.2:c.210T>G	NP_001278849.1:p.Pro70=