Canonical Allele Identifier: CA2366796851
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs1979988960

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726811C>T , CM000682.2:g.46726811C>T GRCh38
NC_000020.10:g.45355450C>T , CM000682.1:g.45355450C>T GRCh37
NC_000020.9:g.44788857C>T NCBI36
NG_016284.1:g.22172C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1289-53C>T MANE Select ENSP00000352216.2:n.1289-53C>T
ENST00000359271.3:c.1289-53C>T ENSP00000352216.2:n.1289-53C>T
NM_030777.3:c.1289-53C>T NP_110404.1:n.1289-53C>T
XM_011529060.1:c.1352-53C>T XP_011527362.1:n.1352-53C>T
XM_011529061.1:c.1298-53C>T XP_011527363.1:n.1298-53C>T
XM_011529062.1:c.1352-4C>T XP_011527364.1:n.1352-4C>T
XM_011529063.1:c.1352-53C>T XP_011527365.1:n.1352-53C>T
XM_011529064.1:c.1352-4C>T XP_011527366.1:n.1352-4C>T
XM_011529065.1:c.1352-53C>T XP_011527367.1:n.1352-53C>T
XR_936641.1:n.1488-4C>T
XM_011529060.2:c.1352-53C>T XP_011527362.1:n.1352-53C>T
XM_011529061.2:c.1298-53C>T XP_011527363.1:n.1298-53C>T
XM_011529062.2:c.1352-4C>T XP_011527364.1:n.1352-4C>T
XM_011529063.2:c.1352-53C>T XP_011527365.1:n.1352-53C>T
XM_011529064.2:c.1352-4C>T XP_011527366.1:n.1352-4C>T
XM_011529065.2:c.1352-53C>T XP_011527367.1:n.1352-53C>T
XM_017028087.2:c.1289-53C>T XP_016883576.1:n.1289-53C>T
XR_936641.2:n.1475-4C>T
NM_030777.4:c.1289-53C>T MANE Select NP_110404.1:n.1289-53C>T