Canonical Allele Identifier: CA744919117
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs1206415890

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46724870_46724871insAGGACGGA , CM000682.2:g.46724870_46724871insAGGACGGA GRCh38
NC_000020.10:g.45353509_45353510insAGGACGGA , CM000682.1:g.45353509_45353510insAGGACGGA GRCh37
NC_000020.9:g.44786916_44786917insAGGACGGA NCBI36
NG_016284.1:g.20231_20232insAGGACGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.5-171_5-170insAGGACGGA MANE Select ENSP00000352216.2:n.5-171_5-170insAGGACGGA
ENST00000359271.3:c.5-171_5-170insAGGACGGA ENSP00000352216.2:n.5-171_5-170insAGGACGGA
ENST00000611837.1:n.157-171_157-170insAGGACGGA
NM_030777.3:c.5-171_5-170insAGGACGGA NP_110404.1:n.5-171_5-170insAGGACGGA
XM_011529060.1:c.68-171_68-170insAGGACGGA XP_011527362.1:n.68-171_68-170insAGGACGGA
XM_011529061.1:c.14-171_14-170insAGGACGGA XP_011527363.1:n.14-171_14-170insAGGACGGA
XM_011529062.1:c.68-171_68-170insAGGACGGA XP_011527364.1:n.68-171_68-170insAGGACGGA
XM_011529063.1:c.68-171_68-170insAGGACGGA XP_011527365.1:n.68-171_68-170insAGGACGGA
XM_011529064.1:c.68-171_68-170insAGGACGGA XP_011527366.1:n.68-171_68-170insAGGACGGA
XM_011529065.1:c.68-171_68-170insAGGACGGA XP_011527367.1:n.68-171_68-170insAGGACGGA
XR_936641.1:n.204-171_204-170insAGGACGGA
XM_011529060.2:c.68-171_68-170insAGGACGGA XP_011527362.1:n.68-171_68-170insAGGACGGA
XM_011529061.2:c.14-171_14-170insAGGACGGA XP_011527363.1:n.14-171_14-170insAGGACGGA
XM_011529062.2:c.68-171_68-170insAGGACGGA XP_011527364.1:n.68-171_68-170insAGGACGGA
XM_011529063.2:c.68-171_68-170insAGGACGGA XP_011527365.1:n.68-171_68-170insAGGACGGA
XM_011529064.2:c.68-171_68-170insAGGACGGA XP_011527366.1:n.68-171_68-170insAGGACGGA
XM_011529065.2:c.68-171_68-170insAGGACGGA XP_011527367.1:n.68-171_68-170insAGGACGGA
XM_017028087.2:c.5-171_5-170insAGGACGGA XP_016883576.1:n.5-171_5-170insAGGACGGA
XR_936641.2:n.191-171_191-170insAGGACGGA
NM_030777.4:c.5-171_5-170insAGGACGGA MANE Select NP_110404.1:n.5-171_5-170insAGGACGGA