Canonical Allele Identifier: CA409267577

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 841511
• ClinVar RCV Id: RCV001043749 ; RCV001759754 ; RCV003160312
• dbSNP Id: rs1269438372
• gnomAD v2: 20-45354321-T-A
• gnomAD v3: 20-46725682-T-A
• gnomAD v4: 20-46725682-T-A
• MyVariant Identifiers: chr20:g.45354321T>A (hg19) ; chr20:g.46725682T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725682T>A , CM000682.2:g.46725682T>A	GRCh38
NC_000020.10:g.45354321T>A , CM000682.1:g.45354321T>A	GRCh37
NC_000020.9:g.44787728T>A	NCBI36
NG_016284.1:g.21043T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.646T>A MANE Select	ENSP00000352216.2:p.Tyr216Asn
ENST00000359271.3:c.646T>A	ENSP00000352216.2:p.Tyr216Asn
NM_030777.3:c.646T>A	NP_110404.1:p.Tyr216Asn
XM_011529060.1:c.709T>A	XP_011527362.1:p.Tyr237Asn
XM_011529061.1:c.655T>A	XP_011527363.1:p.Tyr219Asn
XM_011529062.1:c.709T>A	XP_011527364.1:p.Tyr237Asn
XM_011529063.1:c.709T>A	XP_011527365.1:p.Tyr237Asn
XM_011529064.1:c.709T>A	XP_011527366.1:p.Tyr237Asn
XM_011529065.1:c.709T>A	XP_011527367.1:p.Tyr237Asn
XR_936641.1:n.845T>A
XM_011529060.2:c.709T>A	XP_011527362.1:p.Tyr237Asn
XM_011529061.2:c.655T>A	XP_011527363.1:p.Tyr219Asn
XM_011529062.2:c.709T>A	XP_011527364.1:p.Tyr237Asn
XM_011529063.2:c.709T>A	XP_011527365.1:p.Tyr237Asn
XM_011529064.2:c.709T>A	XP_011527366.1:p.Tyr237Asn
XM_011529065.2:c.709T>A	XP_011527367.1:p.Tyr237Asn
XM_017028087.2:c.646T>A	XP_016883576.1:p.Tyr216Asn
XR_936641.2:n.832T>A
NM_030777.4:c.646T>A MANE Select	NP_110404.1:p.Tyr216Asn