Canonical Allele Identifier: CA2653172042
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46727003C>A , CM000682.2:g.46727003C>A GRCh38
NC_000020.10:g.45355642C>A , CM000682.1:g.45355642C>A GRCh37
NC_000020.9:g.44789049C>A NCBI36
NG_016284.1:g.22364C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1411+17C>A MANE Select ENSP00000352216.2:n.1411+17C>A
ENST00000359271.3:c.1411+17C>A ENSP00000352216.2:n.1411+17C>A
NM_030777.3:c.1411+17C>A NP_110404.1:n.1411+17C>A
XM_011529060.1:c.1474+17C>A XP_011527362.1:n.1474+17C>A
XM_011529061.1:c.1420+17C>A XP_011527363.1:n.1420+17C>A
XM_011529062.1:c.1523+17C>A XP_011527364.1:n.1523+17C>A
XM_011529063.1:c.1474+17C>A XP_011527365.1:n.1474+17C>A
XM_011529064.1:c.1523+17C>A XP_011527366.1:n.1523+17C>A
XM_011529065.1:c.1474+17C>A XP_011527367.1:n.1474+17C>A
XR_936641.1:n.1659+17C>A
XM_011529060.2:c.1474+17C>A XP_011527362.1:n.1474+17C>A
XM_011529061.2:c.1420+17C>A XP_011527363.1:n.1420+17C>A
XM_011529062.2:c.1523+17C>A XP_011527364.1:n.1523+17C>A
XM_011529063.2:c.1474+17C>A XP_011527365.1:n.1474+17C>A
XM_011529064.2:c.1523+17C>A XP_011527366.1:n.1523+17C>A
XM_011529065.2:c.1474+17C>A XP_011527367.1:n.1474+17C>A
XM_017028087.2:c.1411+17C>A XP_016883576.1:n.1411+17C>A
XR_936641.2:n.1646+17C>A
NM_030777.4:c.1411+17C>A MANE Select NP_110404.1:n.1411+17C>A