Canonical Allele Identifier: CA409267423

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46725647-G-T
• MyVariant Identifiers: chr20:g.45354286G>T (hg19) ; chr20:g.46725647G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725647G>T , CM000682.2:g.46725647G>T	GRCh38
NC_000020.10:g.45354286G>T , CM000682.1:g.45354286G>T	GRCh37
NC_000020.9:g.44787693G>T	NCBI36
NG_016284.1:g.21008G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.611G>T MANE Select	ENSP00000352216.2:p.Gly204Val
ENST00000359271.3:c.611G>T	ENSP00000352216.2:p.Gly204Val
NM_030777.3:c.611G>T	NP_110404.1:p.Gly204Val
XM_011529060.1:c.674G>T	XP_011527362.1:p.Gly225Val
XM_011529061.1:c.620G>T	XP_011527363.1:p.Gly207Val
XM_011529062.1:c.674G>T	XP_011527364.1:p.Gly225Val
XM_011529063.1:c.674G>T	XP_011527365.1:p.Gly225Val
XM_011529064.1:c.674G>T	XP_011527366.1:p.Gly225Val
XM_011529065.1:c.674G>T	XP_011527367.1:p.Gly225Val
XR_936641.1:n.810G>T
XM_011529060.2:c.674G>T	XP_011527362.1:p.Gly225Val
XM_011529061.2:c.620G>T	XP_011527363.1:p.Gly207Val
XM_011529062.2:c.674G>T	XP_011527364.1:p.Gly225Val
XM_011529063.2:c.674G>T	XP_011527365.1:p.Gly225Val
XM_011529064.2:c.674G>T	XP_011527366.1:p.Gly225Val
XM_011529065.2:c.674G>T	XP_011527367.1:p.Gly225Val
XM_017028087.2:c.611G>T	XP_016883576.1:p.Gly204Val
XR_936641.2:n.797G>T
NM_030777.4:c.611G>T MANE Select	NP_110404.1:p.Gly204Val