Canonical Allele Identifier: CA340265
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 4586
ClinVar RCV Id: RCV000004848
dbSNP Id: rs587776599
MyVariant Identifiers: chr20:g.45354636del (hg19) chr20:g.46725997del (hg38)
PubMed: PMID:16550171 PMID:25392904
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725997del , CM000682.2:g.46725997del GRCh38
NC_000020.10:g.45354636del , CM000682.1:g.45354636del GRCh37
NC_000020.9:g.44788043del NCBI36
NG_016284.1:g.21358del

Transcript Alleles

HGVS Amino-acid change
ENST00000359271.4:c.961del MANE Select ENSP00000352216.2:p.Val321CysfsTer?
ENST00000359271.3:c.961del ENSP00000352216.2:p.Val321CysfsTer?
NM_030777.3:c.961del NP_110404.1:p.Val321CysfsTer?
XM_011529060.1:c.1024del XP_011527362.1:p.Val342CysfsTer?
XM_011529061.1:c.970del XP_011527363.1:p.Val324CysfsTer?
XM_011529062.1:c.1024del XP_011527364.1:p.Val342CysfsTer?
XM_011529063.1:c.1024del XP_011527365.1:p.Val342CysfsTer?
XM_011529064.1:c.1024del XP_011527366.1:p.Val342CysfsTer?
XM_011529065.1:c.1024del XP_011527367.1:p.Val342CysfsTer?
XR_936641.1:n.1160del
XM_011529060.2:c.1024del XP_011527362.1:p.Val342CysfsTer?
XM_011529061.2:c.970del XP_011527363.1:p.Val324CysfsTer?
XM_011529062.2:c.1024del XP_011527364.1:p.Val342CysfsTer?
XM_011529063.2:c.1024del XP_011527365.1:p.Val342CysfsTer?
XM_011529064.2:c.1024del XP_011527366.1:p.Val342CysfsTer?
XM_011529065.2:c.1024del XP_011527367.1:p.Val342CysfsTer?
XM_017028087.2:c.961del XP_016883576.1:p.Val321CysfsTer?
XR_936641.2:n.1147del
NM_030777.4:c.961del MANE Select NP_110404.1:p.Val321CysfsTer?
Search 100 bp 5'
Search 100 bp 3'