Canonical Allele Identifier: CA1017976581
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46724898_46724918del , CM000682.2:g.46724898_46724918del GRCh38
NC_000020.10:g.45353537_45353557del , CM000682.1:g.45353537_45353557del GRCh37
NC_000020.9:g.44786944_44786964del NCBI36
NG_016284.1:g.20259_20279del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.5-143_5-123del MANE Select ENSP00000352216.2:n.5-143_5-123del
ENST00000359271.3:c.5-143_5-123del ENSP00000352216.2:n.5-143_5-123del
ENST00000611837.1:n.157-143_157-123del
NM_030777.3:c.5-143_5-123del NP_110404.1:n.5-143_5-123del
XM_011529060.1:c.68-143_68-123del XP_011527362.1:n.68-143_68-123del
XM_011529061.1:c.14-143_14-123del XP_011527363.1:n.14-143_14-123del
XM_011529062.1:c.68-143_68-123del XP_011527364.1:n.68-143_68-123del
XM_011529063.1:c.68-143_68-123del XP_011527365.1:n.68-143_68-123del
XM_011529064.1:c.68-143_68-123del XP_011527366.1:n.68-143_68-123del
XM_011529065.1:c.68-143_68-123del XP_011527367.1:n.68-143_68-123del
XR_936641.1:n.204-143_204-123del
XM_011529060.2:c.68-143_68-123del XP_011527362.1:n.68-143_68-123del
XM_011529061.2:c.14-143_14-123del XP_011527363.1:n.14-143_14-123del
XM_011529062.2:c.68-143_68-123del XP_011527364.1:n.68-143_68-123del
XM_011529063.2:c.68-143_68-123del XP_011527365.1:n.68-143_68-123del
XM_011529064.2:c.68-143_68-123del XP_011527366.1:n.68-143_68-123del
XM_011529065.2:c.68-143_68-123del XP_011527367.1:n.68-143_68-123del
XM_017028087.2:c.5-143_5-123del XP_016883576.1:n.5-143_5-123del
XR_936641.2:n.191-143_191-123del
NM_030777.4:c.5-143_5-123del MANE Select NP_110404.1:n.5-143_5-123del