Canonical Allele Identifier: CA409267832
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725724G>C , CM000682.2:g.46725724G>C GRCh38
NC_000020.10:g.45354363G>C , CM000682.1:g.45354363G>C GRCh37
NC_000020.9:g.44787770G>C NCBI36
NG_016284.1:g.21085G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.688G>C MANE Select ENSP00000352216.2:p.Gly230Arg
ENST00000359271.3:c.688G>C ENSP00000352216.2:p.Gly230Arg
NM_030777.3:c.688G>C NP_110404.1:p.Gly230Arg
XM_011529060.1:c.751G>C XP_011527362.1:p.Gly251Arg
XM_011529061.1:c.697G>C XP_011527363.1:p.Gly233Arg
XM_011529062.1:c.751G>C XP_011527364.1:p.Gly251Arg
XM_011529063.1:c.751G>C XP_011527365.1:p.Gly251Arg
XM_011529064.1:c.751G>C XP_011527366.1:p.Gly251Arg
XM_011529065.1:c.751G>C XP_011527367.1:p.Gly251Arg
XR_936641.1:n.887G>C
XM_011529060.2:c.751G>C XP_011527362.1:p.Gly251Arg
XM_011529061.2:c.697G>C XP_011527363.1:p.Gly233Arg
XM_011529062.2:c.751G>C XP_011527364.1:p.Gly251Arg
XM_011529063.2:c.751G>C XP_011527365.1:p.Gly251Arg
XM_011529064.2:c.751G>C XP_011527366.1:p.Gly251Arg
XM_011529065.2:c.751G>C XP_011527367.1:p.Gly251Arg
XM_017028087.2:c.688G>C XP_016883576.1:p.Gly230Arg
XR_936641.2:n.874G>C
NM_030777.4:c.688G>C MANE Select NP_110404.1:p.Gly230Arg