Canonical Allele Identifier: CA510848250
Community Standard Title: NM_030777.4(SLC2A10):c.1032C>T (p.Asp344=)
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726068C>T , CM000682.2:g.46726068C>T GRCh38
NC_000020.10:g.45354707C>T , CM000682.1:g.45354707C>T GRCh37
NC_000020.9:g.44788114C>T NCBI36
NG_016284.1:g.21429C>T

Transcript Alleles

HGVS Amino-acid Change
NM_030777.4:c.1032C>T MANE Select NP_110404.1:p.Asp344=
ENST00000359271.4:c.1032C>T MANE Select ENSP00000352216.2:p.Asp344=
NM_030777.3:c.1032C>T NP_110404.1:p.Asp344=
ENST00000359271.3:c.1032C>T ENSP00000352216.2:p.Asp344=
XM_011529060.1:c.1095C>T XP_011527362.1:p.Asp365=
XM_011529060.2:c.1095C>T XP_011527362.1:p.Asp365=
XM_011529061.1:c.1041C>T XP_011527363.1:p.Asp347=
XM_011529061.2:c.1041C>T XP_011527363.1:p.Asp347=
XM_011529062.1:c.1095C>T XP_011527364.1:p.Asp365=
XM_011529062.2:c.1095C>T XP_011527364.1:p.Asp365=
XM_011529063.1:c.1095C>T XP_011527365.1:p.Asp365=
XM_011529063.2:c.1095C>T XP_011527365.1:p.Asp365=
XM_011529064.1:c.1095C>T XP_011527366.1:p.Asp365=
XM_011529064.2:c.1095C>T XP_011527366.1:p.Asp365=
XM_011529065.1:c.1095C>T XP_011527367.1:p.Asp365=
XM_011529065.2:c.1095C>T XP_011527367.1:p.Asp365=
XM_017028087.2:c.1032C>T XP_016883576.1:p.Asp344=
XR_936641.1:n.1231C>T
XR_936641.2:n.1218C>T