Canonical Allele Identifier: CA320537

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 213720
• ClinVar RCV Id: RCV000196120 ; RCV000340579 ; RCV001171030
• dbSNP Id: rs139932041
• ExAC: 20:45354606 G / A
• gnomAD v2: 20-45354606-G-A
• gnomAD v3: 20-46725967-G-A
• gnomAD v4: 20-46725967-G-A
• COSMIC: COSM4099049
• MyVariant Identifiers: chr20:g.45354606G>A (hg19) ; chr20:g.46725967G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725967G>A , CM000682.2:g.46725967G>A	GRCh38
NC_000020.10:g.45354606G>A , CM000682.1:g.45354606G>A	GRCh37
NC_000020.9:g.44788013G>A	NCBI36
NG_016284.1:g.21328G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.931G>A MANE Select	ENSP00000352216.2:p.Val311Ile
ENST00000359271.3:c.931G>A	ENSP00000352216.2:p.Val311Ile
NM_030777.3:c.931G>A	NP_110404.1:p.Val311Ile
XM_011529060.1:c.994G>A	XP_011527362.1:p.Val332Ile
XM_011529061.1:c.940G>A	XP_011527363.1:p.Val314Ile
XM_011529062.1:c.994G>A	XP_011527364.1:p.Val332Ile
XM_011529063.1:c.994G>A	XP_011527365.1:p.Val332Ile
XM_011529064.1:c.994G>A	XP_011527366.1:p.Val332Ile
XM_011529065.1:c.994G>A	XP_011527367.1:p.Val332Ile
XR_936641.1:n.1130G>A
XM_011529060.2:c.994G>A	XP_011527362.1:p.Val332Ile
XM_011529061.2:c.940G>A	XP_011527363.1:p.Val314Ile
XM_011529062.2:c.994G>A	XP_011527364.1:p.Val332Ile
XM_011529063.2:c.994G>A	XP_011527365.1:p.Val332Ile
XM_011529064.2:c.994G>A	XP_011527366.1:p.Val332Ile
XM_011529065.2:c.994G>A	XP_011527367.1:p.Val332Ile
XM_017028087.2:c.931G>A	XP_016883576.1:p.Val311Ile
XR_936641.2:n.1117G>A
NM_030777.4:c.931G>A MANE Select	NP_110404.1:p.Val311Ile