Canonical Allele Identifier: CA2816531410

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725635del , CM000682.2:g.46725635del	GRCh38
NC_000020.10:g.45354274del , CM000682.1:g.45354274del	GRCh37
NC_000020.9:g.44787681del	NCBI36
NG_016284.1:g.20996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.599del MANE Select	ENSP00000352216.2:p.Pro200HisfsTer?
ENST00000359271.3:c.599del	ENSP00000352216.2:p.Pro200HisfsTer?
NM_030777.3:c.599del	NP_110404.1:p.Pro200HisfsTer?
XM_011529060.1:c.662del	XP_011527362.1:p.Pro221HisfsTer?
XM_011529061.1:c.608del	XP_011527363.1:p.Pro203HisfsTer?
XM_011529062.1:c.662del	XP_011527364.1:p.Pro221HisfsTer?
XM_011529063.1:c.662del	XP_011527365.1:p.Pro221HisfsTer?
XM_011529064.1:c.662del	XP_011527366.1:p.Pro221HisfsTer?
XM_011529065.1:c.662del	XP_011527367.1:p.Pro221HisfsTer?
XR_936641.1:n.798del
XM_011529060.2:c.662del	XP_011527362.1:p.Pro221HisfsTer?
XM_011529061.2:c.608del	XP_011527363.1:p.Pro203HisfsTer?
XM_011529062.2:c.662del	XP_011527364.1:p.Pro221HisfsTer?
XM_011529063.2:c.662del	XP_011527365.1:p.Pro221HisfsTer?
XM_011529064.2:c.662del	XP_011527366.1:p.Pro221HisfsTer?
XM_011529065.2:c.662del	XP_011527367.1:p.Pro221HisfsTer?
XM_017028087.2:c.599del	XP_016883576.1:p.Pro200HisfsTer?
XR_936641.2:n.785del
NM_030777.4:c.599del MANE Select	NP_110404.1:p.Pro200HisfsTer?