Canonical Allele Identifier: CA2366795899
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46724861_46724862delinsAG , CM000682.2:g.46724861_46724862delinsAG GRCh38
NC_000020.10:g.45353500_45353501delinsAG , CM000682.1:g.45353500_45353501delinsAG GRCh37
NC_000020.9:g.44786907_44786908delinsAG NCBI36
NG_016284.1:g.20222_20223delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.5-180_5-179delinsAG MANE Select ENSP00000352216.2:n.5-180_5-179delinsAG
ENST00000359271.3:c.5-180_5-179delinsAG ENSP00000352216.2:n.5-180_5-179delinsAG
ENST00000611837.1:n.157-180_157-179delinsAG
NM_030777.3:c.5-180_5-179delinsAG NP_110404.1:n.5-180_5-179delinsAG
XM_011529060.1:c.68-180_68-179delinsAG XP_011527362.1:n.68-180_68-179delinsAG
XM_011529061.1:c.14-180_14-179delinsAG XP_011527363.1:n.14-180_14-179delinsAG
XM_011529062.1:c.68-180_68-179delinsAG XP_011527364.1:n.68-180_68-179delinsAG
XM_011529063.1:c.68-180_68-179delinsAG XP_011527365.1:n.68-180_68-179delinsAG
XM_011529064.1:c.68-180_68-179delinsAG XP_011527366.1:n.68-180_68-179delinsAG
XM_011529065.1:c.68-180_68-179delinsAG XP_011527367.1:n.68-180_68-179delinsAG
XR_936641.1:n.204-180_204-179delinsAG
XM_011529060.2:c.68-180_68-179delinsAG XP_011527362.1:n.68-180_68-179delinsAG
XM_011529061.2:c.14-180_14-179delinsAG XP_011527363.1:n.14-180_14-179delinsAG
XM_011529062.2:c.68-180_68-179delinsAG XP_011527364.1:n.68-180_68-179delinsAG
XM_011529063.2:c.68-180_68-179delinsAG XP_011527365.1:n.68-180_68-179delinsAG
XM_011529064.2:c.68-180_68-179delinsAG XP_011527366.1:n.68-180_68-179delinsAG
XM_011529065.2:c.68-180_68-179delinsAG XP_011527367.1:n.68-180_68-179delinsAG
XM_017028087.2:c.5-180_5-179delinsAG XP_016883576.1:n.5-180_5-179delinsAG
XR_936641.2:n.191-180_191-179delinsAG
NM_030777.4:c.5-180_5-179delinsAG MANE Select NP_110404.1:n.5-180_5-179delinsAG