Canonical Allele Identifier: CA409271655

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1181704892
• gnomAD v2: 20-45355509-G-C
• gnomAD v3: 20-46726870-G-C
• gnomAD v4: 20-46726870-G-C
• MyVariant Identifiers: chr20:g.45355509G>C (hg19) ; chr20:g.46726870G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726870G>C , CM000682.2:g.46726870G>C	GRCh38
NC_000020.10:g.45355509G>C , CM000682.1:g.45355509G>C	GRCh37
NC_000020.9:g.44788916G>C	NCBI36
NG_016284.1:g.22231G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1295G>C MANE Select	ENSP00000352216.2:p.Trp432Ser
ENST00000359271.3:c.1295G>C	ENSP00000352216.2:p.Trp432Ser
NM_030777.3:c.1295G>C	NP_110404.1:p.Trp432Ser
XM_011529060.1:c.1358G>C	XP_011527362.1:p.Trp453Ser
XM_011529061.1:c.1304G>C	XP_011527363.1:p.Trp435Ser
XM_011529062.1:c.1407G>C	XP_011527364.1:p.Leu469=
XM_011529063.1:c.1358G>C	XP_011527365.1:p.Trp453Ser
XM_011529064.1:c.1407G>C	XP_011527366.1:p.Leu469=
XM_011529065.1:c.1358G>C	XP_011527367.1:p.Trp453Ser
XR_936641.1:n.1543G>C
XM_011529060.2:c.1358G>C	XP_011527362.1:p.Trp453Ser
XM_011529061.2:c.1304G>C	XP_011527363.1:p.Trp435Ser
XM_011529062.2:c.1407G>C	XP_011527364.1:p.Leu469=
XM_011529063.2:c.1358G>C	XP_011527365.1:p.Trp453Ser
XM_011529064.2:c.1407G>C	XP_011527366.1:p.Leu469=
XM_011529065.2:c.1358G>C	XP_011527367.1:p.Trp453Ser
XM_017028087.2:c.1295G>C	XP_016883576.1:p.Trp432Ser
XR_936641.2:n.1530G>C
NM_030777.4:c.1295G>C MANE Select	NP_110404.1:p.Trp432Ser