Canonical Allele Identifier: CA409272181

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46726963-G-T
• MyVariant Identifiers: chr20:g.45355602G>T (hg19) ; chr20:g.46726963G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726963G>T , CM000682.2:g.46726963G>T	GRCh38
NC_000020.10:g.45355602G>T , CM000682.1:g.45355602G>T	GRCh37
NC_000020.9:g.44789009G>T	NCBI36
NG_016284.1:g.22324G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.1388G>T MANE Select	ENSP00000352216.2:p.Ser463Ile
ENST00000359271.3:c.1388G>T	ENSP00000352216.2:p.Ser463Ile
NM_030777.3:c.1388G>T	NP_110404.1:p.Ser463Ile
XM_011529060.1:c.1451G>T	XP_011527362.1:p.Ser484Ile
XM_011529061.1:c.1397G>T	XP_011527363.1:p.Ser466Ile
XM_011529062.1:c.1500G>T	XP_011527364.1:p.Gln500His
XM_011529063.1:c.1451G>T	XP_011527365.1:p.Ser484Ile
XM_011529064.1:c.1500G>T	XP_011527366.1:p.Gln500His
XM_011529065.1:c.1451G>T	XP_011527367.1:p.Ser484Ile
XR_936641.1:n.1636G>T
XM_011529060.2:c.1451G>T	XP_011527362.1:p.Ser484Ile
XM_011529061.2:c.1397G>T	XP_011527363.1:p.Ser466Ile
XM_011529062.2:c.1500G>T	XP_011527364.1:p.Gln500His
XM_011529063.2:c.1451G>T	XP_011527365.1:p.Ser484Ile
XM_011529064.2:c.1500G>T	XP_011527366.1:p.Gln500His
XM_011529065.2:c.1451G>T	XP_011527367.1:p.Ser484Ile
XM_017028087.2:c.1388G>T	XP_016883576.1:p.Ser463Ile
XR_936641.2:n.1623G>T
NM_030777.4:c.1388G>T MANE Select	NP_110404.1:p.Ser463Ile