Canonical Allele Identifier: CA2816531380

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725208dup , CM000682.2:g.46725208dup	GRCh38
NC_000020.10:g.45353847dup , CM000682.1:g.45353847dup	GRCh37
NC_000020.9:g.44787254dup	NCBI36
NG_016284.1:g.20569dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.172dup MANE Select	ENSP00000352216.2:p.Ala58GlyfsTer13
ENST00000359271.3:c.172dup	ENSP00000352216.2:p.Ala58GlyfsTer13
ENST00000611837.1:n.324dup
NM_030777.3:c.172dup	NP_110404.1:p.Ala58GlyfsTer13
XM_011529060.1:c.235dup	XP_011527362.1:p.Ala79GlyfsTer13
XM_011529061.1:c.181dup	XP_011527363.1:p.Ala61GlyfsTer13
XM_011529062.1:c.235dup	XP_011527364.1:p.Ala79GlyfsTer13
XM_011529063.1:c.235dup	XP_011527365.1:p.Ala79GlyfsTer13
XM_011529064.1:c.235dup	XP_011527366.1:p.Ala79GlyfsTer13
XM_011529065.1:c.235dup	XP_011527367.1:p.Ala79GlyfsTer13
XR_936641.1:n.371dup
XM_011529060.2:c.235dup	XP_011527362.1:p.Ala79GlyfsTer13
XM_011529061.2:c.181dup	XP_011527363.1:p.Ala61GlyfsTer13
XM_011529062.2:c.235dup	XP_011527364.1:p.Ala79GlyfsTer13
XM_011529063.2:c.235dup	XP_011527365.1:p.Ala79GlyfsTer13
XM_011529064.2:c.235dup	XP_011527366.1:p.Ala79GlyfsTer13
XM_011529065.2:c.235dup	XP_011527367.1:p.Ala79GlyfsTer13
XM_017028087.2:c.172dup	XP_016883576.1:p.Ala58GlyfsTer13
XR_936641.2:n.358dup
NM_030777.4:c.172dup MANE Select	NP_110404.1:p.Ala58GlyfsTer13