Canonical Allele Identifier: CA315754808

Gene: SLC2A10

Linked Data

• dbSNP Id: rs776588446

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724850dup , CM000682.2:g.46724850dup	GRCh38
NC_000020.10:g.45353489dup , CM000682.1:g.45353489dup	GRCh37
NC_000020.9:g.44786896dup	NCBI36
NG_016284.1:g.20211dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-191dup MANE Select	ENSP00000352216.2:n.5-191dup
ENST00000359271.3:c.5-191dup	ENSP00000352216.2:n.5-191dup
ENST00000611837.1:n.157-191dup
NM_030777.3:c.5-191dup	NP_110404.1:n.5-191dup
XM_011529060.1:c.68-191dup	XP_011527362.1:n.68-191dup
XM_011529061.1:c.14-191dup	XP_011527363.1:n.14-191dup
XM_011529062.1:c.68-191dup	XP_011527364.1:n.68-191dup
XM_011529063.1:c.68-191dup	XP_011527365.1:n.68-191dup
XM_011529064.1:c.68-191dup	XP_011527366.1:n.68-191dup
XM_011529065.1:c.68-191dup	XP_011527367.1:n.68-191dup
XR_936641.1:n.204-191dup
XM_011529060.2:c.68-191dup	XP_011527362.1:n.68-191dup
XM_011529061.2:c.14-191dup	XP_011527363.1:n.14-191dup
XM_011529062.2:c.68-191dup	XP_011527364.1:n.68-191dup
XM_011529063.2:c.68-191dup	XP_011527365.1:n.68-191dup
XM_011529064.2:c.68-191dup	XP_011527366.1:n.68-191dup
XM_011529065.2:c.68-191dup	XP_011527367.1:n.68-191dup
XM_017028087.2:c.5-191dup	XP_016883576.1:n.5-191dup
XR_936641.2:n.191-191dup
NM_030777.4:c.5-191dup MANE Select	NP_110404.1:n.5-191dup