Canonical Allele Identifier: CA9892161

Gene: SLC2A10

Linked Data

• dbSNP Id: rs781576507
• ExAC: 20:45355510 G / T
• gnomAD v2: 20-45355510-G-T
• gnomAD v4: 20-46726871-G-T
• MyVariant Identifiers: chr20:g.45355510G>T (hg19) ; chr20:g.46726871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726871G>T , CM000682.2:g.46726871G>T	GRCh38
NC_000020.10:g.45355510G>T , CM000682.1:g.45355510G>T	GRCh37
NC_000020.9:g.44788917G>T	NCBI36
NG_016284.1:g.22232G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1296G>T MANE Select	ENSP00000352216.2:p.Trp432Cys
ENST00000359271.3:c.1296G>T	ENSP00000352216.2:p.Trp432Cys
NM_030777.3:c.1296G>T	NP_110404.1:p.Trp432Cys
XM_011529060.1:c.1359G>T	XP_011527362.1:p.Trp453Cys
XM_011529061.1:c.1305G>T	XP_011527363.1:p.Trp435Cys
XM_011529062.1:c.1408G>T	XP_011527364.1:p.Ala470Ser
XM_011529063.1:c.1359G>T	XP_011527365.1:p.Trp453Cys
XM_011529064.1:c.1408G>T	XP_011527366.1:p.Ala470Ser
XM_011529065.1:c.1359G>T	XP_011527367.1:p.Trp453Cys
XR_936641.1:n.1544G>T
XM_011529060.2:c.1359G>T	XP_011527362.1:p.Trp453Cys
XM_011529061.2:c.1305G>T	XP_011527363.1:p.Trp435Cys
XM_011529062.2:c.1408G>T	XP_011527364.1:p.Ala470Ser
XM_011529063.2:c.1359G>T	XP_011527365.1:p.Trp453Cys
XM_011529064.2:c.1408G>T	XP_011527366.1:p.Ala470Ser
XM_011529065.2:c.1359G>T	XP_011527367.1:p.Trp453Cys
XM_017028087.2:c.1296G>T	XP_016883576.1:p.Trp432Cys
XR_936641.2:n.1531G>T
NM_030777.4:c.1296G>T MANE Select	NP_110404.1:p.Trp432Cys