Canonical Allele Identifier: CA636177764

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1205159786
• gnomAD v2: 20-45354234-GC-G
• gnomAD v3: 20-46725595-GC-G
• gnomAD v4: 20-46725595-GC-G
• MyVariant Identifiers: chr20:g.45354235del (hg19) ; chr20:g.46725596del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725596del , CM000682.2:g.46725596del	GRCh38
NC_000020.10:g.45354235del , CM000682.1:g.45354235del	GRCh37
NC_000020.9:g.44787642del	NCBI36
NG_016284.1:g.20957del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.560del MANE Select	ENSP00000352216.2:p.Ala187ValfsTer?
ENST00000359271.3:c.560del	ENSP00000352216.2:p.Ala187ValfsTer?
NM_030777.3:c.560del	NP_110404.1:p.Ala187ValfsTer?
XM_011529060.1:c.623del	XP_011527362.1:p.Ala208ValfsTer?
XM_011529061.1:c.569del	XP_011527363.1:p.Ala190ValfsTer?
XM_011529062.1:c.623del	XP_011527364.1:p.Ala208ValfsTer?
XM_011529063.1:c.623del	XP_011527365.1:p.Ala208ValfsTer?
XM_011529064.1:c.623del	XP_011527366.1:p.Ala208ValfsTer?
XM_011529065.1:c.623del	XP_011527367.1:p.Ala208ValfsTer?
XR_936641.1:n.759del
XM_011529060.2:c.623del	XP_011527362.1:p.Ala208ValfsTer?
XM_011529061.2:c.569del	XP_011527363.1:p.Ala190ValfsTer?
XM_011529062.2:c.623del	XP_011527364.1:p.Ala208ValfsTer?
XM_011529063.2:c.623del	XP_011527365.1:p.Ala208ValfsTer?
XM_011529064.2:c.623del	XP_011527366.1:p.Ala208ValfsTer?
XM_011529065.2:c.623del	XP_011527367.1:p.Ala208ValfsTer?
XM_017028087.2:c.560del	XP_016883576.1:p.Ala187ValfsTer?
XR_936641.2:n.746del
NM_030777.4:c.560del MANE Select	NP_110404.1:p.Ala187ValfsTer?