Canonical Allele Identifier: CA636057117

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1339663248
• gnomAD v2: 20-45353651-AC-A
• gnomAD v4: 20-46725012-AC-A
• MyVariant Identifiers: chr20:g.45353652del (hg19) ; chr20:g.46725013del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725013del , CM000682.2:g.46725013del	GRCh38
NC_000020.10:g.45353652del , CM000682.1:g.45353652del	GRCh37
NC_000020.9:g.44787059del	NCBI36
NG_016284.1:g.20374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-28del MANE Select	ENSP00000352216.2:n.5-28del
ENST00000359271.3:c.5-28del	ENSP00000352216.2:n.5-28del
ENST00000611837.1:n.157-28del
NM_030777.3:c.5-28del	NP_110404.1:n.5-28del
XM_011529060.1:c.68-28del	XP_011527362.1:n.68-28del
XM_011529061.1:c.14-28del	XP_011527363.1:n.14-28del
XM_011529062.1:c.68-28del	XP_011527364.1:n.68-28del
XM_011529063.1:c.68-28del	XP_011527365.1:n.68-28del
XM_011529064.1:c.68-28del	XP_011527366.1:n.68-28del
XM_011529065.1:c.68-28del	XP_011527367.1:n.68-28del
XR_936641.1:n.204-28del
XM_011529060.2:c.68-28del	XP_011527362.1:n.68-28del
XM_011529061.2:c.14-28del	XP_011527363.1:n.14-28del
XM_011529062.2:c.68-28del	XP_011527364.1:n.68-28del
XM_011529063.2:c.68-28del	XP_011527365.1:n.68-28del
XM_011529064.2:c.68-28del	XP_011527366.1:n.68-28del
XM_011529065.2:c.68-28del	XP_011527367.1:n.68-28del
XM_017028087.2:c.5-28del	XP_016883576.1:n.5-28del
XR_936641.2:n.191-28del
NM_030777.4:c.5-28del MANE Select	NP_110404.1:n.5-28del