Canonical Allele Identifier: CA2816531378

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725155_46725161del , CM000682.2:g.46725155_46725161del	GRCh38
NC_000020.10:g.45353794_45353800del , CM000682.1:g.45353794_45353800del	GRCh37
NC_000020.9:g.44787201_44787207del	NCBI36
NG_016284.1:g.20516_20522del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.119_125del MANE Select	ENSP00000352216.2:p.Phe40Ter
ENST00000359271.3:c.119_125del	ENSP00000352216.2:p.Phe40Ter
ENST00000611837.1:n.271_277del
NM_030777.3:c.119_125del	NP_110404.1:p.Phe40Ter
XM_011529060.1:c.182_188del	XP_011527362.1:p.Phe61Ter
XM_011529061.1:c.128_134del	XP_011527363.1:p.Phe43Ter
XM_011529062.1:c.182_188del	XP_011527364.1:p.Phe61Ter
XM_011529063.1:c.182_188del	XP_011527365.1:p.Phe61Ter
XM_011529064.1:c.182_188del	XP_011527366.1:p.Phe61Ter
XM_011529065.1:c.182_188del	XP_011527367.1:p.Phe61Ter
XR_936641.1:n.318_324del
XM_011529060.2:c.182_188del	XP_011527362.1:p.Phe61Ter
XM_011529061.2:c.128_134del	XP_011527363.1:p.Phe43Ter
XM_011529062.2:c.182_188del	XP_011527364.1:p.Phe61Ter
XM_011529063.2:c.182_188del	XP_011527365.1:p.Phe61Ter
XM_011529064.2:c.182_188del	XP_011527366.1:p.Phe61Ter
XM_011529065.2:c.182_188del	XP_011527367.1:p.Phe61Ter
XM_017028087.2:c.119_125del	XP_016883576.1:p.Phe40Ter
XR_936641.2:n.305_311del
NM_030777.4:c.119_125del MANE Select	NP_110404.1:p.Phe40Ter