Canonical Allele Identifier: CA2653170901
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725643_46725644del , CM000682.2:g.46725643_46725644del GRCh38
NC_000020.10:g.45354282_45354283del , CM000682.1:g.45354282_45354283del GRCh37
NC_000020.9:g.44787689_44787690del NCBI36
NG_016284.1:g.21004_21005del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.607_608del MANE Select ENSP00000352216.2:p.Gly203ArgfsTer2
ENST00000359271.3:c.607_608del ENSP00000352216.2:p.Gly203ArgfsTer2
NM_030777.3:c.607_608del NP_110404.1:p.Gly203ArgfsTer2
XM_011529060.1:c.670_671del XP_011527362.1:p.Gly224ArgfsTer2
XM_011529061.1:c.616_617del XP_011527363.1:p.Gly206ArgfsTer2
XM_011529062.1:c.670_671del XP_011527364.1:p.Gly224ArgfsTer2
XM_011529063.1:c.670_671del XP_011527365.1:p.Gly224ArgfsTer2
XM_011529064.1:c.670_671del XP_011527366.1:p.Gly224ArgfsTer2
XM_011529065.1:c.670_671del XP_011527367.1:p.Gly224ArgfsTer2
XR_936641.1:n.806_807del
XM_011529060.2:c.670_671del XP_011527362.1:p.Gly224ArgfsTer2
XM_011529061.2:c.616_617del XP_011527363.1:p.Gly206ArgfsTer2
XM_011529062.2:c.670_671del XP_011527364.1:p.Gly224ArgfsTer2
XM_011529063.2:c.670_671del XP_011527365.1:p.Gly224ArgfsTer2
XM_011529064.2:c.670_671del XP_011527366.1:p.Gly224ArgfsTer2
XM_011529065.2:c.670_671del XP_011527367.1:p.Gly224ArgfsTer2
XM_017028087.2:c.607_608del XP_016883576.1:p.Gly203ArgfsTer2
XR_936641.2:n.793_794del
NM_030777.4:c.607_608del MANE Select NP_110404.1:p.Gly203ArgfsTer2