Canonical Allele Identifier: CA323067

Gene: SLC2A10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46729356C>T , CM000682.2:g.46729356C>T	GRCh38
NC_000020.10:g.45357995C>T , CM000682.1:g.45357995C>T	GRCh37
NC_000020.9:g.44791402C>T	NCBI36
NG_016284.1:g.24717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1415C>T MANE Select	ENSP00000352216.2:p.Thr472Ile
ENST00000359271.3:c.1415C>T	ENSP00000352216.2:p.Thr472Ile
NM_030777.3:c.1415C>T	NP_110404.1:p.Thr472Ile
XM_011529060.1:c.1478C>T	XP_011527362.1:p.Thr493Ile
XM_011529061.1:c.1424C>T	XP_011527363.1:p.Thr475Ile
XM_011529062.1:c.1523+2370C>T	XP_011527364.1:n.1523+2370C>T
XM_011529065.1:c.1474+2370C>T	XP_011527367.1:n.1474+2370C>T
XR_936641.1:n.1663C>T
XM_011529060.2:c.1478C>T	XP_011527362.1:p.Thr493Ile
XM_011529061.2:c.1424C>T	XP_011527363.1:p.Thr475Ile
XM_011529062.2:c.1523+2370C>T	XP_011527364.1:n.1523+2370C>T
XM_011529065.2:c.1474+2370C>T	XP_011527367.1:n.1474+2370C>T
XM_017028087.2:c.1411+2370C>T	XP_016883576.1:n.1411+2370C>T
XR_936641.2:n.1650C>T
NM_030777.4:c.1415C>T MANE Select	NP_110404.1:p.Thr472Ile