Canonical Allele Identifier: CA1017976356
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs1979767441

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46724825_46724826insG , CM000682.2:g.46724825_46724826insG GRCh38
NC_000020.10:g.45353464_45353465insG , CM000682.1:g.45353464_45353465insG GRCh37
NC_000020.9:g.44786871_44786872insG NCBI36
NG_016284.1:g.20186_20187insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.5-216_5-215insG MANE Select ENSP00000352216.2:n.5-216_5-215insG
ENST00000359271.3:c.5-216_5-215insG ENSP00000352216.2:n.5-216_5-215insG
ENST00000611837.1:n.157-216_157-215insG
NM_030777.3:c.5-216_5-215insG NP_110404.1:n.5-216_5-215insG
XM_011529060.1:c.68-216_68-215insG XP_011527362.1:n.68-216_68-215insG
XM_011529061.1:c.14-216_14-215insG XP_011527363.1:n.14-216_14-215insG
XM_011529062.1:c.68-216_68-215insG XP_011527364.1:n.68-216_68-215insG
XM_011529063.1:c.68-216_68-215insG XP_011527365.1:n.68-216_68-215insG
XM_011529064.1:c.68-216_68-215insG XP_011527366.1:n.68-216_68-215insG
XM_011529065.1:c.68-216_68-215insG XP_011527367.1:n.68-216_68-215insG
XR_936641.1:n.204-216_204-215insG
XM_011529060.2:c.68-216_68-215insG XP_011527362.1:n.68-216_68-215insG
XM_011529061.2:c.14-216_14-215insG XP_011527363.1:n.14-216_14-215insG
XM_011529062.2:c.68-216_68-215insG XP_011527364.1:n.68-216_68-215insG
XM_011529063.2:c.68-216_68-215insG XP_011527365.1:n.68-216_68-215insG
XM_011529064.2:c.68-216_68-215insG XP_011527366.1:n.68-216_68-215insG
XM_011529065.2:c.68-216_68-215insG XP_011527367.1:n.68-216_68-215insG
XM_017028087.2:c.5-216_5-215insG XP_016883576.1:n.5-216_5-215insG
XR_936641.2:n.191-216_191-215insG
NM_030777.4:c.5-216_5-215insG MANE Select NP_110404.1:n.5-216_5-215insG