Canonical Allele Identifier: CA2695229832
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725354del , CM000682.2:g.46725354del GRCh38
NC_000020.10:g.45353993del , CM000682.1:g.45353993del GRCh37
NC_000020.9:g.44787400del NCBI36
NG_016284.1:g.20715del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.318del MANE Select ENSP00000352216.2:p.Val107TrpfsTer?
ENST00000359271.3:c.318del ENSP00000352216.2:p.Val107TrpfsTer?
ENST00000611837.1:n.470del
NM_030777.3:c.318del NP_110404.1:p.Val107TrpfsTer?
XM_011529060.1:c.381del XP_011527362.1:p.Val128TrpfsTer?
XM_011529061.1:c.327del XP_011527363.1:p.Val110TrpfsTer?
XM_011529062.1:c.381del XP_011527364.1:p.Val128TrpfsTer?
XM_011529063.1:c.381del XP_011527365.1:p.Val128TrpfsTer?
XM_011529064.1:c.381del XP_011527366.1:p.Val128TrpfsTer?
XM_011529065.1:c.381del XP_011527367.1:p.Val128TrpfsTer?
XR_936641.1:n.517del
XM_011529060.2:c.381del XP_011527362.1:p.Val128TrpfsTer?
XM_011529061.2:c.327del XP_011527363.1:p.Val110TrpfsTer?
XM_011529062.2:c.381del XP_011527364.1:p.Val128TrpfsTer?
XM_011529063.2:c.381del XP_011527365.1:p.Val128TrpfsTer?
XM_011529064.2:c.381del XP_011527366.1:p.Val128TrpfsTer?
XM_011529065.2:c.381del XP_011527367.1:p.Val128TrpfsTer?
XM_017028087.2:c.318del XP_016883576.1:p.Val107TrpfsTer?
XR_936641.2:n.504del
NM_030777.4:c.318del MANE Select NP_110404.1:p.Val107TrpfsTer?