Canonical Allele Identifier: CA409267632

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45354330C>A (hg19) ; chr20:g.46725691C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725691C>A , CM000682.2:g.46725691C>A	GRCh38
NC_000020.10:g.45354330C>A , CM000682.1:g.45354330C>A	GRCh37
NC_000020.9:g.44787737C>A	NCBI36
NG_016284.1:g.21052C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.655C>A MANE Select	ENSP00000352216.2:p.Leu219Met
ENST00000359271.3:c.655C>A	ENSP00000352216.2:p.Leu219Met
NM_030777.3:c.655C>A	NP_110404.1:p.Leu219Met
XM_011529060.1:c.718C>A	XP_011527362.1:p.Leu240Met
XM_011529061.1:c.664C>A	XP_011527363.1:p.Leu222Met
XM_011529062.1:c.718C>A	XP_011527364.1:p.Leu240Met
XM_011529063.1:c.718C>A	XP_011527365.1:p.Leu240Met
XM_011529064.1:c.718C>A	XP_011527366.1:p.Leu240Met
XM_011529065.1:c.718C>A	XP_011527367.1:p.Leu240Met
XR_936641.1:n.854C>A
XM_011529060.2:c.718C>A	XP_011527362.1:p.Leu240Met
XM_011529061.2:c.664C>A	XP_011527363.1:p.Leu222Met
XM_011529062.2:c.718C>A	XP_011527364.1:p.Leu240Met
XM_011529063.2:c.718C>A	XP_011527365.1:p.Leu240Met
XM_011529064.2:c.718C>A	XP_011527366.1:p.Leu240Met
XM_011529065.2:c.718C>A	XP_011527367.1:p.Leu240Met
XM_017028087.2:c.655C>A	XP_016883576.1:p.Leu219Met
XR_936641.2:n.841C>A
NM_030777.4:c.655C>A MANE Select	NP_110404.1:p.Leu219Met