Canonical Allele Identifier: CA2573157154

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 1609874
• ClinVar RCV Id: RCV002155350
• dbSNP Id: rs2123041402

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725032_46725035del , CM000682.2:g.46725032_46725035del	GRCh38
NC_000020.10:g.45353671_45353674del , CM000682.1:g.45353671_45353674del	GRCh37
NC_000020.9:g.44787078_44787081del	NCBI36
NG_016284.1:g.20393_20396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-9_5-6del MANE Select	ENSP00000352216.2:n.5-9_5-6del
ENST00000359271.3:c.5-9_5-6del	ENSP00000352216.2:n.5-9_5-6del
ENST00000611837.1:n.157-9_157-6del
NM_030777.3:c.5-9_5-6del	NP_110404.1:n.5-9_5-6del
XM_011529060.1:c.68-9_68-6del	XP_011527362.1:n.68-9_68-6del
XM_011529061.1:c.14-9_14-6del	XP_011527363.1:n.14-9_14-6del
XM_011529062.1:c.68-9_68-6del	XP_011527364.1:n.68-9_68-6del
XM_011529063.1:c.68-9_68-6del	XP_011527365.1:n.68-9_68-6del
XM_011529064.1:c.68-9_68-6del	XP_011527366.1:n.68-9_68-6del
XM_011529065.1:c.68-9_68-6del	XP_011527367.1:n.68-9_68-6del
XR_936641.1:n.204-9_204-6del
XM_011529060.2:c.68-9_68-6del	XP_011527362.1:n.68-9_68-6del
XM_011529061.2:c.14-9_14-6del	XP_011527363.1:n.14-9_14-6del
XM_011529062.2:c.68-9_68-6del	XP_011527364.1:n.68-9_68-6del
XM_011529063.2:c.68-9_68-6del	XP_011527365.1:n.68-9_68-6del
XM_011529064.2:c.68-9_68-6del	XP_011527366.1:n.68-9_68-6del
XM_011529065.2:c.68-9_68-6del	XP_011527367.1:n.68-9_68-6del
XM_017028087.2:c.5-9_5-6del	XP_016883576.1:n.5-9_5-6del
XR_936641.2:n.191-9_191-6del
NM_030777.4:c.5-9_5-6del MANE Select	NP_110404.1:n.5-9_5-6del