Canonical Allele Identifier: CA375452092

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300030G>C (hg19) ; chr9:g.134408184G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408184G>C , CM000671.2:g.134408184G>C	GRCh38
NC_000009.11:g.137300030G>C , CM000671.1:g.137300030G>C	GRCh37
NC_000009.10:g.136439851G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.315G>C MANE Select	ENSP00000419692.1:p.Glu105Asp
ENST00000672570.1:c.234G>C	ENSP00000500402.1:p.Glu78Asp
ENST00000356384.4:n.725G>C
ENST00000481739.1:c.315G>C	ENSP00000419692.1:p.Glu105Asp
NM_001291920.1:c.234G>C	NP_001278849.1:p.Glu78Asp
NM_001291921.1:c.24G>C	NP_001278850.1:p.Glu8Asp
NM_002957.5:c.315G>C	NP_002948.1:p.Glu105Asp
NM_002957.6:c.315G>C MANE Select	NP_002948.1:p.Glu105Asp
NM_001291921.2:c.24G>C	NP_001278850.1:p.Glu8Asp
NM_001291920.2:c.234G>C	NP_001278849.1:p.Glu78Asp