Canonical Allele Identifier: CA9891939

Gene: SLC2A10

Linked Data

• dbSNP Id: rs778104155
• ExAC: 20:45353922 T / A
• gnomAD v2: 20-45353922-T-A
• gnomAD v4: 20-46725283-T-A
• MyVariant Identifiers: chr20:g.45353922T>A (hg19) ; chr20:g.46725283T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725283T>A , CM000682.2:g.46725283T>A	GRCh38
NC_000020.10:g.45353922T>A , CM000682.1:g.45353922T>A	GRCh37
NC_000020.9:g.44787329T>A	NCBI36
NG_016284.1:g.20644T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.247T>A MANE Select	ENSP00000352216.2:p.Leu83Met
ENST00000359271.3:c.247T>A	ENSP00000352216.2:p.Leu83Met
ENST00000611837.1:n.399T>A
NM_030777.3:c.247T>A	NP_110404.1:p.Leu83Met
XM_011529060.1:c.310T>A	XP_011527362.1:p.Leu104Met
XM_011529061.1:c.256T>A	XP_011527363.1:p.Leu86Met
XM_011529062.1:c.310T>A	XP_011527364.1:p.Leu104Met
XM_011529063.1:c.310T>A	XP_011527365.1:p.Leu104Met
XM_011529064.1:c.310T>A	XP_011527366.1:p.Leu104Met
XM_011529065.1:c.310T>A	XP_011527367.1:p.Leu104Met
XR_936641.1:n.446T>A
XM_011529060.2:c.310T>A	XP_011527362.1:p.Leu104Met
XM_011529061.2:c.256T>A	XP_011527363.1:p.Leu86Met
XM_011529062.2:c.310T>A	XP_011527364.1:p.Leu104Met
XM_011529063.2:c.310T>A	XP_011527365.1:p.Leu104Met
XM_011529064.2:c.310T>A	XP_011527366.1:p.Leu104Met
XM_011529065.2:c.310T>A	XP_011527367.1:p.Leu104Met
XM_017028087.2:c.247T>A	XP_016883576.1:p.Leu83Met
XR_936641.2:n.433T>A
NM_030777.4:c.247T>A MANE Select	NP_110404.1:p.Leu83Met