Canonical Allele Identifier: CA2697547414

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 2761376
• ClinVar RCV Id: RCV003503234

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725379_46725868delinsC , CM000682.2:g.46725379_46725868delinsC	GRCh38
NC_000020.10:g.45354018_45354507delinsC , CM000682.1:g.45354018_45354507delinsC	GRCh37
NC_000020.9:g.44787425_44787914delinsC	NCBI36
NG_016284.1:g.20740_21229delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.343_832delinsC MANE Select	ENSP00000352216.2:p.Ser115_Ala278delinsPro
ENST00000359271.3:c.343_832delinsC	ENSP00000352216.2:p.Ser115_Ala278delinsPro
NM_030777.3:c.343_832delinsC	NP_110404.1:p.Ser115_Ala278delinsPro
XM_011529060.1:c.406_895delinsC	XP_011527362.1:p.Ser136_Ala299delinsPro
XM_011529061.1:c.352_841delinsC	XP_011527363.1:p.Ser118_Ala281delinsPro
XM_011529062.1:c.406_895delinsC	XP_011527364.1:p.Ser136_Ala299delinsPro
XM_011529063.1:c.406_895delinsC	XP_011527365.1:p.Ser136_Ala299delinsPro
XM_011529064.1:c.406_895delinsC	XP_011527366.1:p.Ser136_Ala299delinsPro
XM_011529065.1:c.406_895delinsC	XP_011527367.1:p.Ser136_Ala299delinsPro
XR_936641.1:n.542_1031delinsC
XM_011529060.2:c.406_895delinsC	XP_011527362.1:p.Ser136_Ala299delinsPro
XM_011529061.2:c.352_841delinsC	XP_011527363.1:p.Ser118_Ala281delinsPro
XM_011529062.2:c.406_895delinsC	XP_011527364.1:p.Ser136_Ala299delinsPro
XM_011529063.2:c.406_895delinsC	XP_011527365.1:p.Ser136_Ala299delinsPro
XM_011529064.2:c.406_895delinsC	XP_011527366.1:p.Ser136_Ala299delinsPro
XM_011529065.2:c.406_895delinsC	XP_011527367.1:p.Ser136_Ala299delinsPro
XM_017028087.2:c.343_832delinsC	XP_016883576.1:p.Ser115_Ala278delinsPro
XR_936641.2:n.529_1018delinsC
NM_030777.4:c.343_832delinsC MANE Select	NP_110404.1:p.Ser115_Ala278delinsPro