Canonical Allele Identifier: CA1017977597
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs1980014355

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46727054_46727056dup , CM000682.2:g.46727054_46727056dup GRCh38
NC_000020.10:g.45355693_45355695dup , CM000682.1:g.45355693_45355695dup GRCh37
NC_000020.9:g.44789100_44789102dup NCBI36
NG_016284.1:g.22415_22417dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1411+68_1411+70dup MANE Select ENSP00000352216.2:n.1411+68_1411+70dup
ENST00000359271.3:c.1411+68_1411+70dup ENSP00000352216.2:n.1411+68_1411+70dup
NM_030777.3:c.1411+68_1411+70dup NP_110404.1:n.1411+68_1411+70dup
XM_011529060.1:c.1474+68_1474+70dup XP_011527362.1:n.1474+68_1474+70dup
XM_011529061.1:c.1420+68_1420+70dup XP_011527363.1:n.1420+68_1420+70dup
XM_011529062.1:c.1523+68_1523+70dup XP_011527364.1:n.1523+68_1523+70dup
XM_011529063.1:c.1474+68_1474+70dup XP_011527365.1:n.1474+68_1474+70dup
XM_011529064.1:c.1523+68_1523+70dup XP_011527366.1:n.1523+68_1523+70dup
XM_011529065.1:c.1474+68_1474+70dup XP_011527367.1:n.1474+68_1474+70dup
XR_936641.1:n.1659+68_1659+70dup
XM_011529060.2:c.1474+68_1474+70dup XP_011527362.1:n.1474+68_1474+70dup
XM_011529061.2:c.1420+68_1420+70dup XP_011527363.1:n.1420+68_1420+70dup
XM_011529062.2:c.1523+68_1523+70dup XP_011527364.1:n.1523+68_1523+70dup
XM_011529063.2:c.1474+68_1474+70dup XP_011527365.1:n.1474+68_1474+70dup
XM_011529064.2:c.1523+68_1523+70dup XP_011527366.1:n.1523+68_1523+70dup
XM_011529065.2:c.1474+68_1474+70dup XP_011527367.1:n.1474+68_1474+70dup
XM_017028087.2:c.1411+68_1411+70dup XP_016883576.1:n.1411+68_1411+70dup
XR_936641.2:n.1646+68_1646+70dup
NM_030777.4:c.1411+68_1411+70dup MANE Select NP_110404.1:n.1411+68_1411+70dup