Canonical Allele Identifier: CA343472811

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389118T>G (hg19) ; chr1:g.165419881T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419881T>G , CM000663.2:g.165419881T>G	GRCh38
NC_000001.10:g.165389118T>G , CM000663.1:g.165389118T>G	GRCh37
NC_000001.9:g.163655742T>G	NCBI36
NG_029517.1:g.30475A>C
NG_029517.2:g.30475A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.431A>C MANE Select	ENSP00000352900.5:p.Asp144Ala
ENST00000359842.9:c.431A>C	ENSP00000352900.5:p.Asp144Ala
ENST00000470566.1:n.356A>C
ENST00000619224.1:c.62A>C	ENSP00000482458.1:p.Asp21Ala
NM_001256570.1:c.62A>C	NP_001243499.1:p.Asp21Ala
NM_001256571.1:c.62A>C	NP_001243500.1:p.Asp21Ala
NM_006917.4:c.431A>C	NP_008848.1:p.Asp144Ala
NM_006917.5:c.431A>C MANE Select	NP_008848.1:p.Asp144Ala
NM_001256571.2:c.62A>C	NP_001243500.1:p.Asp21Ala
NM_001256570.2:c.62A>C	NP_001243499.1:p.Asp21Ala