Canonical Allele Identifier: CA636177761

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1365040228
• gnomAD v2: 20-45354124-CCTATGCCCTCAA-C
• gnomAD v4: 20-46725485-CCTATGCCCTCAA-C
• MyVariant Identifiers: chr20:g.45354125_45354136del (hg19) ; chr20:g.46725486_46725497del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725492_46725503del , CM000682.2:g.46725492_46725503del	GRCh38
NC_000020.10:g.45354131_45354142del , CM000682.1:g.45354131_45354142del	GRCh37
NC_000020.9:g.44787538_44787549del	NCBI36
NG_016284.1:g.20853_20864del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.456_467del MANE Select	ENSP00000352216.2:p.Leu153_Ala156del
ENST00000359271.3:c.456_467del	ENSP00000352216.2:p.Leu153_Ala156del
NM_030777.3:c.456_467del	NP_110404.1:p.Leu153_Ala156del
XM_011529060.1:c.519_530del	XP_011527362.1:p.Leu174_Ala177del
XM_011529061.1:c.465_476del	XP_011527363.1:p.Leu156_Ala159del
XM_011529062.1:c.519_530del	XP_011527364.1:p.Leu174_Ala177del
XM_011529063.1:c.519_530del	XP_011527365.1:p.Leu174_Ala177del
XM_011529064.1:c.519_530del	XP_011527366.1:p.Leu174_Ala177del
XM_011529065.1:c.519_530del	XP_011527367.1:p.Leu174_Ala177del
XR_936641.1:n.655_666del
XM_011529060.2:c.519_530del	XP_011527362.1:p.Leu174_Ala177del
XM_011529061.2:c.465_476del	XP_011527363.1:p.Leu156_Ala159del
XM_011529062.2:c.519_530del	XP_011527364.1:p.Leu174_Ala177del
XM_011529063.2:c.519_530del	XP_011527365.1:p.Leu174_Ala177del
XM_011529064.2:c.519_530del	XP_011527366.1:p.Leu174_Ala177del
XM_011529065.2:c.519_530del	XP_011527367.1:p.Leu174_Ala177del
XM_017028087.2:c.456_467del	XP_016883576.1:p.Leu153_Ala156del
XR_936641.2:n.642_653del
NM_030777.4:c.456_467del MANE Select	NP_110404.1:p.Leu153_Ala156del