Canonical Allele Identifier: CA409271798

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45355528C>G (hg19) ; chr20:g.46726889C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726889C>G , CM000682.2:g.46726889C>G	GRCh38
NC_000020.10:g.45355528C>G , CM000682.1:g.45355528C>G	GRCh37
NC_000020.9:g.44788935C>G	NCBI36
NG_016284.1:g.22250C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1314C>G MANE Select	ENSP00000352216.2:p.Ile438Met
ENST00000359271.3:c.1314C>G	ENSP00000352216.2:p.Ile438Met
NM_030777.3:c.1314C>G	NP_110404.1:p.Ile438Met
XM_011529060.1:c.1377C>G	XP_011527362.1:p.Ile459Met
XM_011529061.1:c.1323C>G	XP_011527363.1:p.Ile441Met
XM_011529062.1:c.1426C>G	XP_011527364.1:p.Leu476Val
XM_011529063.1:c.1377C>G	XP_011527365.1:p.Ile459Met
XM_011529064.1:c.1426C>G	XP_011527366.1:p.Leu476Val
XM_011529065.1:c.1377C>G	XP_011527367.1:p.Ile459Met
XR_936641.1:n.1562C>G
XM_011529060.2:c.1377C>G	XP_011527362.1:p.Ile459Met
XM_011529061.2:c.1323C>G	XP_011527363.1:p.Ile441Met
XM_011529062.2:c.1426C>G	XP_011527364.1:p.Leu476Val
XM_011529063.2:c.1377C>G	XP_011527365.1:p.Ile459Met
XM_011529064.2:c.1426C>G	XP_011527366.1:p.Leu476Val
XM_011529065.2:c.1377C>G	XP_011527367.1:p.Ile459Met
XM_017028087.2:c.1314C>G	XP_016883576.1:p.Ile438Met
XR_936641.2:n.1549C>G
NM_030777.4:c.1314C>G MANE Select	NP_110404.1:p.Ile438Met