Canonical Allele Identifier: CA744899181

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1307084999
• gnomAD v4: 20-46726801-C-T
• MyVariant Identifiers: chr20:g.45355440C>T (hg19) ; chr20:g.46726801C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726801C>T , CM000682.2:g.46726801C>T	GRCh38
NC_000020.10:g.45355440C>T , CM000682.1:g.45355440C>T	GRCh37
NC_000020.9:g.44788847C>T	NCBI36
NG_016284.1:g.22162C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-63C>T MANE Select	ENSP00000352216.2:n.1289-63C>T
ENST00000359271.3:c.1289-63C>T	ENSP00000352216.2:n.1289-63C>T
NM_030777.3:c.1289-63C>T	NP_110404.1:n.1289-63C>T
XM_011529060.1:c.1352-63C>T	XP_011527362.1:n.1352-63C>T
XM_011529061.1:c.1298-63C>T	XP_011527363.1:n.1298-63C>T
XM_011529062.1:c.1352-14C>T	XP_011527364.1:n.1352-14C>T
XM_011529063.1:c.1352-63C>T	XP_011527365.1:n.1352-63C>T
XM_011529064.1:c.1352-14C>T	XP_011527366.1:n.1352-14C>T
XM_011529065.1:c.1352-63C>T	XP_011527367.1:n.1352-63C>T
XR_936641.1:n.1488-14C>T
XM_011529060.2:c.1352-63C>T	XP_011527362.1:n.1352-63C>T
XM_011529061.2:c.1298-63C>T	XP_011527363.1:n.1298-63C>T
XM_011529062.2:c.1352-14C>T	XP_011527364.1:n.1352-14C>T
XM_011529063.2:c.1352-63C>T	XP_011527365.1:n.1352-63C>T
XM_011529064.2:c.1352-14C>T	XP_011527366.1:n.1352-14C>T
XM_011529065.2:c.1352-63C>T	XP_011527367.1:n.1352-63C>T
XM_017028087.2:c.1289-63C>T	XP_016883576.1:n.1289-63C>T
XR_936641.2:n.1475-14C>T
NM_030777.4:c.1289-63C>T MANE Select	NP_110404.1:n.1289-63C>T