Canonical Allele Identifier: CA9892223

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46729394A>G , CM000682.2:g.46729394A>G	GRCh38
NC_000020.10:g.45358033A>G , CM000682.1:g.45358033A>G	GRCh37
NC_000020.9:g.44791440A>G	NCBI36
NG_016284.1:g.24755A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.1453A>G MANE Select	NP_110404.1:p.Thr485Ala
ENST00000359271.4:c.1453A>G MANE Select	ENSP00000352216.2:p.Thr485Ala
NM_030777.3:c.1453A>G	NP_110404.1:p.Thr485Ala
ENST00000359271.3:c.1453A>G	ENSP00000352216.2:p.Thr485Ala
XM_011529060.1:c.1516A>G	XP_011527362.1:p.Thr506Ala
XM_011529060.2:c.1516A>G	XP_011527362.1:p.Thr506Ala
XM_011529061.1:c.1462A>G	XP_011527363.1:p.Thr488Ala
XM_011529061.2:c.1462A>G	XP_011527363.1:p.Thr488Ala
XM_011529062.1:c.1523+2408A>G	XP_011527364.1:n.1523+2408A>G
XM_011529062.2:c.1523+2408A>G	XP_011527364.1:n.1523+2408A>G
XM_011529065.1:c.1474+2408A>G	XP_011527367.1:n.1474+2408A>G
XM_011529065.2:c.1474+2408A>G	XP_011527367.1:n.1474+2408A>G
XM_017028087.2:c.1411+2408A>G	XP_016883576.1:n.1411+2408A>G
XR_936641.1:n.1701A>G
XR_936641.2:n.1688A>G