Canonical Allele Identifier: CA510771278

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46726898-G-A
• MyVariant Identifiers: chr20:g.45355537G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726898G>A , CM000682.2:g.46726898G>A	GRCh38
NC_000020.10:g.45355537G>A , CM000682.1:g.45355537G>A	GRCh37
NC_000020.9:g.44788944G>A	NCBI36
NG_016284.1:g.22259G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1323G>A MANE Select	ENSP00000352216.2:p.Val441=
ENST00000359271.3:c.1323G>A	ENSP00000352216.2:p.Val441=
NM_030777.3:c.1323G>A	NP_110404.1:p.Val441=
XM_011529060.1:c.1386G>A	XP_011527362.1:p.Val462=
XM_011529061.1:c.1332G>A	XP_011527363.1:p.Val444=
XM_011529062.1:c.1435G>A	XP_011527364.1:p.Gly479Arg
XM_011529063.1:c.1386G>A	XP_011527365.1:p.Val462=
XM_011529064.1:c.1435G>A	XP_011527366.1:p.Gly479Arg
XM_011529065.1:c.1386G>A	XP_011527367.1:p.Val462=
XR_936641.1:n.1571G>A
XM_011529060.2:c.1386G>A	XP_011527362.1:p.Val462=
XM_011529061.2:c.1332G>A	XP_011527363.1:p.Val444=
XM_011529062.2:c.1435G>A	XP_011527364.1:p.Gly479Arg
XM_011529063.2:c.1386G>A	XP_011527365.1:p.Val462=
XM_011529064.2:c.1435G>A	XP_011527366.1:p.Gly479Arg
XM_011529065.2:c.1386G>A	XP_011527367.1:p.Val462=
XM_017028087.2:c.1323G>A	XP_016883576.1:p.Val441=
XR_936641.2:n.1558G>A
NM_030777.4:c.1323G>A MANE Select	NP_110404.1:p.Val441=