Canonical Allele Identifier: CA375452635

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300117C>G (hg19) ; chr9:g.134408271C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408271C>G , CM000671.2:g.134408271C>G	GRCh38
NC_000009.11:g.137300117C>G , CM000671.1:g.137300117C>G	GRCh37
NC_000009.10:g.136439938C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.402C>G MANE Select	ENSP00000419692.1:p.Ile134Met
ENST00000672570.1:c.321C>G	ENSP00000500402.1:p.Ile107Met
ENST00000356384.4:n.812C>G
ENST00000481739.1:c.402C>G	ENSP00000419692.1:p.Ile134Met
NM_001291920.1:c.321C>G	NP_001278849.1:p.Ile107Met
NM_001291921.1:c.111C>G	NP_001278850.1:p.Ile37Met
NM_002957.5:c.402C>G	NP_002948.1:p.Ile134Met
NM_002957.6:c.402C>G MANE Select	NP_002948.1:p.Ile134Met
NM_001291921.2:c.111C>G	NP_001278850.1:p.Ile37Met
NM_001291920.2:c.321C>G	NP_001278849.1:p.Ile107Met