Canonical Allele Identifier: CA293556

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46729482A>G , CM000682.2:g.46729482A>G	GRCh38
NC_000020.10:g.45358121A>G , CM000682.1:g.45358121A>G	GRCh37
NC_000020.9:g.44791528A>G	NCBI36
NG_016284.1:g.24843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1541A>G MANE Select	ENSP00000352216.2:p.Lys514Arg
ENST00000359271.3:c.1541A>G	ENSP00000352216.2:p.Lys514Arg
NM_030777.3:c.1541A>G	NP_110404.1:p.Lys514Arg
XM_011529060.1:c.1604A>G	XP_011527362.1:p.Lys535Arg
XM_011529061.1:c.1550A>G	XP_011527363.1:p.Lys517Arg
XM_011529062.1:c.1523+2496A>G	XP_011527364.1:n.1523+2496A>G
XM_011529065.1:c.1474+2496A>G	XP_011527367.1:n.1474+2496A>G
XR_936641.1:n.1789A>G
XM_011529060.2:c.1604A>G	XP_011527362.1:p.Lys535Arg
XM_011529061.2:c.1550A>G	XP_011527363.1:p.Lys517Arg
XM_011529062.2:c.1523+2496A>G	XP_011527364.1:n.1523+2496A>G
XM_011529065.2:c.1474+2496A>G	XP_011527367.1:n.1474+2496A>G
XM_017028087.2:c.1411+2496A>G	XP_016883576.1:n.1411+2496A>G
XR_936641.2:n.1776A>G
NM_030777.4:c.1541A>G MANE Select	NP_110404.1:p.Lys514Arg