Canonical Allele Identifier: CA9892112

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726198C>T , CM000682.2:g.46726198C>T	GRCh38
NC_000020.10:g.45354837C>T , CM000682.1:g.45354837C>T	GRCh37
NC_000020.9:g.44788244C>T	NCBI36
NG_016284.1:g.21559C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.1162C>T MANE Select	NP_110404.1:p.Arg388Trp
ENST00000359271.4:c.1162C>T MANE Select	ENSP00000352216.2:p.Arg388Trp
NM_030777.3:c.1162C>T	NP_110404.1:p.Arg388Trp
ENST00000359271.3:c.1162C>T	ENSP00000352216.2:p.Arg388Trp
XM_011529060.1:c.1225C>T	XP_011527362.1:p.Arg409Trp
XM_011529060.2:c.1225C>T	XP_011527362.1:p.Arg409Trp
XM_011529061.1:c.1171C>T	XP_011527363.1:p.Arg391Trp
XM_011529061.2:c.1171C>T	XP_011527363.1:p.Arg391Trp
XM_011529062.1:c.1225C>T	XP_011527364.1:p.Arg409Trp
XM_011529062.2:c.1225C>T	XP_011527364.1:p.Arg409Trp
XM_011529063.1:c.1225C>T	XP_011527365.1:p.Arg409Trp
XM_011529063.2:c.1225C>T	XP_011527365.1:p.Arg409Trp
XM_011529064.1:c.1225C>T	XP_011527366.1:p.Arg409Trp
XM_011529064.2:c.1225C>T	XP_011527366.1:p.Arg409Trp
XM_011529065.1:c.1225C>T	XP_011527367.1:p.Arg409Trp
XM_011529065.2:c.1225C>T	XP_011527367.1:p.Arg409Trp
XM_017028087.2:c.1162C>T	XP_016883576.1:p.Arg388Trp
XR_936641.1:n.1361C>T
XR_936641.2:n.1348C>T