Canonical Allele Identifier: CA343472838

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389130G>T (hg19) ; chr1:g.165419893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419893G>T , CM000663.2:g.165419893G>T	GRCh38
NC_000001.10:g.165389130G>T , CM000663.1:g.165389130G>T	GRCh37
NC_000001.9:g.163655754G>T	NCBI36
NG_029517.1:g.30463C>A
NG_029517.2:g.30463C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359842.10:c.419C>A MANE Select	ENSP00000352900.5:p.Ala140Asp
ENST00000359842.9:c.419C>A	ENSP00000352900.5:p.Ala140Asp
ENST00000470566.1:n.344C>A
ENST00000619224.1:c.50C>A	ENSP00000482458.1:p.Ala17Asp
NM_001256570.1:c.50C>A	NP_001243499.1:p.Ala17Asp
NM_001256571.1:c.50C>A	NP_001243500.1:p.Ala17Asp
NM_006917.4:c.419C>A	NP_008848.1:p.Ala140Asp
NM_006917.5:c.419C>A MANE Select	NP_008848.1:p.Ala140Asp
NM_001256571.2:c.50C>A	NP_001243500.1:p.Ala17Asp
NM_001256570.2:c.50C>A	NP_001243499.1:p.Ala17Asp