Canonical Allele Identifier: CA343472790

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389109G>A (hg19) ; chr1:g.165419872G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419872G>A , CM000663.2:g.165419872G>A	GRCh38
NC_000001.10:g.165389109G>A , CM000663.1:g.165389109G>A	GRCh37
NC_000001.9:g.163655733G>A	NCBI36
NG_029517.1:g.30484C>T
NG_029517.2:g.30484C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.440C>T MANE Select	ENSP00000352900.5:p.Ser147Leu
ENST00000359842.9:c.440C>T	ENSP00000352900.5:p.Ser147Leu
ENST00000470566.1:n.365C>T
ENST00000619224.1:c.71C>T	ENSP00000482458.1:p.Ser24Leu
NM_001256570.1:c.71C>T	NP_001243499.1:p.Ser24Leu
NM_001256571.1:c.71C>T	NP_001243500.1:p.Ser24Leu
NM_006917.4:c.440C>T	NP_008848.1:p.Ser147Leu
NM_006917.5:c.440C>T MANE Select	NP_008848.1:p.Ser147Leu
NM_001256571.2:c.71C>T	NP_001243500.1:p.Ser24Leu
NM_001256570.2:c.71C>T	NP_001243499.1:p.Ser24Leu