Canonical Allele Identifier: CA322344

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 213715
• ClinVar RCV Id: RCV000197879
• dbSNP Id: rs863223730
• MyVariant Identifiers: chr20:g.45354310G>C (hg19) ; chr20:g.46725671G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725671G>C , CM000682.2:g.46725671G>C	GRCh38
NC_000020.10:g.45354310G>C , CM000682.1:g.45354310G>C	GRCh37
NC_000020.9:g.44787717G>C	NCBI36
NG_016284.1:g.21032G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.635G>C MANE Select	ENSP00000352216.2:p.Gly212Ala
ENST00000359271.3:c.635G>C	ENSP00000352216.2:p.Gly212Ala
NM_030777.3:c.635G>C	NP_110404.1:p.Gly212Ala
XM_011529060.1:c.698G>C	XP_011527362.1:p.Gly233Ala
XM_011529061.1:c.644G>C	XP_011527363.1:p.Gly215Ala
XM_011529062.1:c.698G>C	XP_011527364.1:p.Gly233Ala
XM_011529063.1:c.698G>C	XP_011527365.1:p.Gly233Ala
XM_011529064.1:c.698G>C	XP_011527366.1:p.Gly233Ala
XM_011529065.1:c.698G>C	XP_011527367.1:p.Gly233Ala
XR_936641.1:n.834G>C
XM_011529060.2:c.698G>C	XP_011527362.1:p.Gly233Ala
XM_011529061.2:c.644G>C	XP_011527363.1:p.Gly215Ala
XM_011529062.2:c.698G>C	XP_011527364.1:p.Gly233Ala
XM_011529063.2:c.698G>C	XP_011527365.1:p.Gly233Ala
XM_011529064.2:c.698G>C	XP_011527366.1:p.Gly233Ala
XM_011529065.2:c.698G>C	XP_011527367.1:p.Gly233Ala
XM_017028087.2:c.635G>C	XP_016883576.1:p.Gly212Ala
XR_936641.2:n.821G>C
NM_030777.4:c.635G>C MANE Select	NP_110404.1:p.Gly212Ala