Canonical Allele Identifier: CA2531312105
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46724783del , CM000682.2:g.46724783del GRCh38
NC_000020.10:g.45353422del , CM000682.1:g.45353422del GRCh37
NC_000020.9:g.44786829del NCBI36
NG_016284.1:g.20144del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.5-258del MANE Select ENSP00000352216.2:n.5-258del
ENST00000359271.3:c.5-258del ENSP00000352216.2:n.5-258del
ENST00000611837.1:n.157-258del
NM_030777.3:c.5-258del NP_110404.1:n.5-258del
XM_011529060.1:c.68-258del XP_011527362.1:n.68-258del
XM_011529061.1:c.14-258del XP_011527363.1:n.14-258del
XM_011529062.1:c.68-258del XP_011527364.1:n.68-258del
XM_011529063.1:c.68-258del XP_011527365.1:n.68-258del
XM_011529064.1:c.68-258del XP_011527366.1:n.68-258del
XM_011529065.1:c.68-258del XP_011527367.1:n.68-258del
XR_936641.1:n.204-258del
XM_011529060.2:c.68-258del XP_011527362.1:n.68-258del
XM_011529061.2:c.14-258del XP_011527363.1:n.14-258del
XM_011529062.2:c.68-258del XP_011527364.1:n.68-258del
XM_011529063.2:c.68-258del XP_011527365.1:n.68-258del
XM_011529064.2:c.68-258del XP_011527366.1:n.68-258del
XM_011529065.2:c.68-258del XP_011527367.1:n.68-258del
XM_017028087.2:c.5-258del XP_016883576.1:n.5-258del
XR_936641.2:n.191-258del
NM_030777.4:c.5-258del MANE Select NP_110404.1:n.5-258del