Canonical Allele Identifier: CA409262051

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46709737A>G , CM000682.2:g.46709737A>G	GRCh38
NC_000020.10:g.45338376A>G , CM000682.1:g.45338376A>G	GRCh37
NC_000020.9:g.44771783A>G	NCBI36
NG_016284.1:g.5098A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.1A>G MANE Select	NP_110404.1:p.Met1Val
ENST00000359271.4:c.1A>G MANE Select	ENSP00000352216.2:p.Met1Val
NM_030777.3:c.1A>G	NP_110404.1:p.Met1Val
ENST00000359271.3:c.1A>G	ENSP00000352216.2:p.Met1Val
ENST00000486000.2:c.1A>G	ENSP00000478679.1:p.Met1Val
XM_011529060.1:c.67+1184A>G	XP_011527362.1:n.67+1184A>G
XM_011529060.2:c.67+1184A>G	XP_011527362.1:n.67+1184A>G
XM_011529062.1:c.67+1184A>G	XP_011527364.1:n.67+1184A>G
XM_011529062.2:c.67+1184A>G	XP_011527364.1:n.67+1184A>G
XM_011529063.1:c.67+1184A>G	XP_011527365.1:n.67+1184A>G
XM_011529063.2:c.67+1184A>G	XP_011527365.1:n.67+1184A>G
XM_011529064.1:c.67+1184A>G	XP_011527366.1:n.67+1184A>G
XM_011529064.2:c.67+1184A>G	XP_011527366.1:n.67+1184A>G
XM_011529065.1:c.67+1184A>G	XP_011527367.1:n.67+1184A>G
XM_011529065.2:c.67+1184A>G	XP_011527367.1:n.67+1184A>G
XM_017028087.2:c.1A>G	XP_016883576.1:p.Met1Val
XR_936641.1:n.203+1184A>G
XR_936641.2:n.190+1184A>G