Canonical Allele Identifier: CA409273084

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46729365T>A , CM000682.2:g.46729365T>A	GRCh38
NC_000020.10:g.45358004T>A , CM000682.1:g.45358004T>A	GRCh37
NC_000020.9:g.44791411T>A	NCBI36
NG_016284.1:g.24726T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.1424T>A MANE Select	NP_110404.1:p.Leu475Ter
ENST00000359271.4:c.1424T>A MANE Select	ENSP00000352216.2:p.Leu475Ter
NM_030777.3:c.1424T>A	NP_110404.1:p.Leu475Ter
ENST00000359271.3:c.1424T>A	ENSP00000352216.2:p.Leu475Ter
XM_011529060.1:c.1487T>A	XP_011527362.1:p.Leu496Ter
XM_011529060.2:c.1487T>A	XP_011527362.1:p.Leu496Ter
XM_011529061.1:c.1433T>A	XP_011527363.1:p.Leu478Ter
XM_011529061.2:c.1433T>A	XP_011527363.1:p.Leu478Ter
XM_011529062.1:c.1523+2379T>A	XP_011527364.1:n.1523+2379T>A
XM_011529062.2:c.1523+2379T>A	XP_011527364.1:n.1523+2379T>A
XM_011529065.1:c.1474+2379T>A	XP_011527367.1:n.1474+2379T>A
XM_011529065.2:c.1474+2379T>A	XP_011527367.1:n.1474+2379T>A
XM_017028087.2:c.1411+2379T>A	XP_016883576.1:n.1411+2379T>A
XR_936641.1:n.1672T>A
XR_936641.2:n.1659T>A