Canonical Allele Identifier: CA9891915
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 659691
dbSNP Id: rs367623970

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725151G>A , CM000682.2:g.46725151G>A GRCh38
NC_000020.10:g.45353790G>A , CM000682.1:g.45353790G>A GRCh37
NC_000020.9:g.44787197G>A NCBI36
NG_016284.1:g.20512G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.115G>A MANE Select ENSP00000352216.2:p.Asp39Asn
ENST00000359271.3:c.115G>A ENSP00000352216.2:p.Asp39Asn
ENST00000611837.1:n.267G>A
NM_030777.3:c.115G>A NP_110404.1:p.Asp39Asn
XM_011529060.1:c.178G>A XP_011527362.1:p.Asp60Asn
XM_011529061.1:c.124G>A XP_011527363.1:p.Asp42Asn
XM_011529062.1:c.178G>A XP_011527364.1:p.Asp60Asn
XM_011529063.1:c.178G>A XP_011527365.1:p.Asp60Asn
XM_011529064.1:c.178G>A XP_011527366.1:p.Asp60Asn
XM_011529065.1:c.178G>A XP_011527367.1:p.Asp60Asn
XR_936641.1:n.314G>A
XM_011529060.2:c.178G>A XP_011527362.1:p.Asp60Asn
XM_011529061.2:c.124G>A XP_011527363.1:p.Asp42Asn
XM_011529062.2:c.178G>A XP_011527364.1:p.Asp60Asn
XM_011529063.2:c.178G>A XP_011527365.1:p.Asp60Asn
XM_011529064.2:c.178G>A XP_011527366.1:p.Asp60Asn
XM_011529065.2:c.178G>A XP_011527367.1:p.Asp60Asn
XM_017028087.2:c.115G>A XP_016883576.1:p.Asp39Asn
XR_936641.2:n.301G>A
NM_030777.4:c.115G>A MANE Select NP_110404.1:p.Asp39Asn