Canonical Allele Identifier: CA2366796879

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1979993524

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726865_46726866insGG , CM000682.2:g.46726865_46726866insGG	GRCh38
NC_000020.10:g.45355504_45355505insGG , CM000682.1:g.45355504_45355505insGG	GRCh37
NC_000020.9:g.44788911_44788912insGG	NCBI36
NG_016284.1:g.22226_22227insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.1290_1291insGG MANE Select	ENSP00000352216.2:p.Thr431GlyfsTer?
ENST00000359271.3:c.1290_1291insGG	ENSP00000352216.2:p.Thr431GlyfsTer?
NM_030777.3:c.1290_1291insGG	NP_110404.1:p.Thr431GlyfsTer?
XM_011529060.1:c.1353_1354insGG	XP_011527362.1:p.Thr452GlyfsTer?
XM_011529061.1:c.1299_1300insGG	XP_011527363.1:p.Thr434GlyfsTer?
XM_011529062.1:c.1402_1403insGG	XP_011527364.1:p.Asp468GlyfsTer?
XM_011529063.1:c.1353_1354insGG	XP_011527365.1:p.Thr452GlyfsTer?
XM_011529064.1:c.1402_1403insGG	XP_011527366.1:p.Asp468GlyfsTer?
XM_011529065.1:c.1353_1354insGG	XP_011527367.1:p.Thr452GlyfsTer?
XR_936641.1:n.1538_1539insGG
XM_011529060.2:c.1353_1354insGG	XP_011527362.1:p.Thr452GlyfsTer?
XM_011529061.2:c.1299_1300insGG	XP_011527363.1:p.Thr434GlyfsTer?
XM_011529062.2:c.1402_1403insGG	XP_011527364.1:p.Asp468GlyfsTer?
XM_011529063.2:c.1353_1354insGG	XP_011527365.1:p.Thr452GlyfsTer?
XM_011529064.2:c.1402_1403insGG	XP_011527366.1:p.Asp468GlyfsTer?
XM_011529065.2:c.1353_1354insGG	XP_011527367.1:p.Thr452GlyfsTer?
XM_017028087.2:c.1290_1291insGG	XP_016883576.1:p.Thr431GlyfsTer?
XR_936641.2:n.1525_1526insGG
NM_030777.4:c.1290_1291insGG MANE Select	NP_110404.1:p.Thr431GlyfsTer?