Canonical Allele Identifier: CA636057843
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs1218841928

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726869_46726870insAC , CM000682.2:g.46726869_46726870insAC GRCh38
NC_000020.10:g.45355508_45355509insAC , CM000682.1:g.45355508_45355509insAC GRCh37
NC_000020.9:g.44788915_44788916insAC NCBI36
NG_016284.1:g.22230_22231insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1294_1295insAC MANE Select ENSP00000352216.2:p.Trp432TyrfsTer?
ENST00000359271.3:c.1294_1295insAC ENSP00000352216.2:p.Trp432TyrfsTer?
NM_030777.3:c.1294_1295insAC NP_110404.1:p.Trp432TyrfsTer?
XM_011529060.1:c.1357_1358insAC XP_011527362.1:p.Trp453TyrfsTer?
XM_011529061.1:c.1303_1304insAC XP_011527363.1:p.Trp435TyrfsTer?
XM_011529062.1:c.1406_1407insAC XP_011527364.1:p.Ala470ArgfsTer?
XM_011529063.1:c.1357_1358insAC XP_011527365.1:p.Trp453TyrfsTer?
XM_011529064.1:c.1406_1407insAC XP_011527366.1:p.Ala470ArgfsTer?
XM_011529065.1:c.1357_1358insAC XP_011527367.1:p.Trp453TyrfsTer?
XR_936641.1:n.1542_1543insAC
XM_011529060.2:c.1357_1358insAC XP_011527362.1:p.Trp453TyrfsTer?
XM_011529061.2:c.1303_1304insAC XP_011527363.1:p.Trp435TyrfsTer?
XM_011529062.2:c.1406_1407insAC XP_011527364.1:p.Ala470ArgfsTer?
XM_011529063.2:c.1357_1358insAC XP_011527365.1:p.Trp453TyrfsTer?
XM_011529064.2:c.1406_1407insAC XP_011527366.1:p.Ala470ArgfsTer?
XM_011529065.2:c.1357_1358insAC XP_011527367.1:p.Trp453TyrfsTer?
XM_017028087.2:c.1294_1295insAC XP_016883576.1:p.Trp432TyrfsTer?
XR_936641.2:n.1529_1530insAC
NM_030777.4:c.1294_1295insAC MANE Select NP_110404.1:p.Trp432TyrfsTer?