Canonical Allele Identifier: CA510847682
Gene: SLC2A10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.45354170G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725531G>A , CM000682.2:g.46725531G>A GRCh38
NC_000020.10:g.45354170G>A , CM000682.1:g.45354170G>A GRCh37
NC_000020.9:g.44787577G>A NCBI36
NG_016284.1:g.20892G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.495G>A MANE Select ENSP00000352216.2:p.Arg165=
ENST00000359271.3:c.495G>A ENSP00000352216.2:p.Arg165=
NM_030777.3:c.495G>A NP_110404.1:p.Arg165=
XM_011529060.1:c.558G>A XP_011527362.1:p.Arg186=
XM_011529061.1:c.504G>A XP_011527363.1:p.Arg168=
XM_011529062.1:c.558G>A XP_011527364.1:p.Arg186=
XM_011529063.1:c.558G>A XP_011527365.1:p.Arg186=
XM_011529064.1:c.558G>A XP_011527366.1:p.Arg186=
XM_011529065.1:c.558G>A XP_011527367.1:p.Arg186=
XR_936641.1:n.694G>A
XM_011529060.2:c.558G>A XP_011527362.1:p.Arg186=
XM_011529061.2:c.504G>A XP_011527363.1:p.Arg168=
XM_011529062.2:c.558G>A XP_011527364.1:p.Arg186=
XM_011529063.2:c.558G>A XP_011527365.1:p.Arg186=
XM_011529064.2:c.558G>A XP_011527366.1:p.Arg186=
XM_011529065.2:c.558G>A XP_011527367.1:p.Arg186=
XM_017028087.2:c.495G>A XP_016883576.1:p.Arg165=
XR_936641.2:n.681G>A
NM_030777.4:c.495G>A MANE Select NP_110404.1:p.Arg165=