Canonical Allele Identifier: CA375452054

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300022A>C (hg19) ; chr9:g.134408176A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408176A>C , CM000671.2:g.134408176A>C	GRCh38
NC_000009.11:g.137300022A>C , CM000671.1:g.137300022A>C	GRCh37
NC_000009.10:g.136439843A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.307A>C MANE Select	ENSP00000419692.1:p.Ser103Arg
ENST00000672570.1:c.226A>C	ENSP00000500402.1:p.Ser76Arg
ENST00000356384.4:n.717A>C
ENST00000481739.1:c.307A>C	ENSP00000419692.1:p.Ser103Arg
NM_001291920.1:c.226A>C	NP_001278849.1:p.Ser76Arg
NM_001291921.1:c.16A>C	NP_001278850.1:p.Ser6Arg
NM_002957.5:c.307A>C	NP_002948.1:p.Ser103Arg
NM_002957.6:c.307A>C MANE Select	NP_002948.1:p.Ser103Arg
NM_001291921.2:c.16A>C	NP_001278850.1:p.Ser6Arg
NM_001291920.2:c.226A>C	NP_001278849.1:p.Ser76Arg