Canonical Allele Identifier: CA315757060

Gene: SLC2A10

Linked Data

• dbSNP Id: rs35102875

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726735dup , CM000682.2:g.46726735dup	GRCh38
NC_000020.10:g.45355374dup , CM000682.1:g.45355374dup	GRCh37
NC_000020.9:g.44788781dup	NCBI36
NG_016284.1:g.22096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-129dup MANE Select	ENSP00000352216.2:n.1289-129dup
ENST00000359271.3:c.1289-129dup	ENSP00000352216.2:n.1289-129dup
NM_030777.3:c.1289-129dup	NP_110404.1:n.1289-129dup
XM_011529060.1:c.1352-129dup	XP_011527362.1:n.1352-129dup
XM_011529061.1:c.1298-129dup	XP_011527363.1:n.1298-129dup
XM_011529062.1:c.1352-80dup	XP_011527364.1:n.1352-80dup
XM_011529063.1:c.1352-129dup	XP_011527365.1:n.1352-129dup
XM_011529064.1:c.1352-80dup	XP_011527366.1:n.1352-80dup
XM_011529065.1:c.1352-129dup	XP_011527367.1:n.1352-129dup
XR_936641.1:n.1488-80dup
XM_011529060.2:c.1352-129dup	XP_011527362.1:n.1352-129dup
XM_011529061.2:c.1298-129dup	XP_011527363.1:n.1298-129dup
XM_011529062.2:c.1352-80dup	XP_011527364.1:n.1352-80dup
XM_011529063.2:c.1352-129dup	XP_011527365.1:n.1352-129dup
XM_011529064.2:c.1352-80dup	XP_011527366.1:n.1352-80dup
XM_011529065.2:c.1352-129dup	XP_011527367.1:n.1352-129dup
XM_017028087.2:c.1289-129dup	XP_016883576.1:n.1289-129dup
XR_936641.2:n.1475-80dup
NM_030777.4:c.1289-129dup MANE Select	NP_110404.1:n.1289-129dup