Canonical Allele Identifier: CA2366796961
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46727010_46727011delinsGT , CM000682.2:g.46727010_46727011delinsGT GRCh38
NC_000020.10:g.45355649_45355650delinsGT , CM000682.1:g.45355649_45355650delinsGT GRCh37
NC_000020.9:g.44789056_44789057delinsGT NCBI36
NG_016284.1:g.22371_22372delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1411+24_1411+25delinsGT MANE Select ENSP00000352216.2:n.1411+24_1411+25delinsGT
ENST00000359271.3:c.1411+24_1411+25delinsGT ENSP00000352216.2:n.1411+24_1411+25delinsGT
NM_030777.3:c.1411+24_1411+25delinsGT NP_110404.1:n.1411+24_1411+25delinsGT
XM_011529060.1:c.1474+24_1474+25delinsGT XP_011527362.1:n.1474+24_1474+25delinsGT
XM_011529061.1:c.1420+24_1420+25delinsGT XP_011527363.1:n.1420+24_1420+25delinsGT
XM_011529062.1:c.1523+24_1523+25delinsGT XP_011527364.1:n.1523+24_1523+25delinsGT
XM_011529063.1:c.1474+24_1474+25delinsGT XP_011527365.1:n.1474+24_1474+25delinsGT
XM_011529064.1:c.1523+24_1523+25delinsGT XP_011527366.1:n.1523+24_1523+25delinsGT
XM_011529065.1:c.1474+24_1474+25delinsGT XP_011527367.1:n.1474+24_1474+25delinsGT
XR_936641.1:n.1659+24_1659+25delinsGT
XM_011529060.2:c.1474+24_1474+25delinsGT XP_011527362.1:n.1474+24_1474+25delinsGT
XM_011529061.2:c.1420+24_1420+25delinsGT XP_011527363.1:n.1420+24_1420+25delinsGT
XM_011529062.2:c.1523+24_1523+25delinsGT XP_011527364.1:n.1523+24_1523+25delinsGT
XM_011529063.2:c.1474+24_1474+25delinsGT XP_011527365.1:n.1474+24_1474+25delinsGT
XM_011529064.2:c.1523+24_1523+25delinsGT XP_011527366.1:n.1523+24_1523+25delinsGT
XM_011529065.2:c.1474+24_1474+25delinsGT XP_011527367.1:n.1474+24_1474+25delinsGT
XM_017028087.2:c.1411+24_1411+25delinsGT XP_016883576.1:n.1411+24_1411+25delinsGT
XR_936641.2:n.1646+24_1646+25delinsGT
NM_030777.4:c.1411+24_1411+25delinsGT MANE Select NP_110404.1:n.1411+24_1411+25delinsGT