Canonical Allele Identifier: CA2366796026

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725074_46725076delinsCTG , CM000682.2:g.46725074_46725076delinsCTG	GRCh38
NC_000020.10:g.45353713_45353715delinsCTG , CM000682.1:g.45353713_45353715delinsCTG	GRCh37
NC_000020.9:g.44787120_44787122delinsCTG	NCBI36
NG_016284.1:g.20435_20437delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.38_40delinsCTG MANE Select	ENSP00000352216.2:p.Ser13=
ENST00000359271.3:c.38_40delinsCTG	ENSP00000352216.2:p.Ser13=
ENST00000611837.1:n.190_192delinsCTG
NM_030777.3:c.38_40delinsCTG	NP_110404.1:p.Ser13=
XM_011529060.1:c.101_103delinsCTG	XP_011527362.1:p.Ser34=
XM_011529061.1:c.47_49delinsCTG	XP_011527363.1:p.Ser16=
XM_011529062.1:c.101_103delinsCTG	XP_011527364.1:p.Ser34=
XM_011529063.1:c.101_103delinsCTG	XP_011527365.1:p.Ser34=
XM_011529064.1:c.101_103delinsCTG	XP_011527366.1:p.Ser34=
XM_011529065.1:c.101_103delinsCTG	XP_011527367.1:p.Ser34=
XR_936641.1:n.237_239delinsCTG
XM_011529060.2:c.101_103delinsCTG	XP_011527362.1:p.Ser34=
XM_011529061.2:c.47_49delinsCTG	XP_011527363.1:p.Ser16=
XM_011529062.2:c.101_103delinsCTG	XP_011527364.1:p.Ser34=
XM_011529063.2:c.101_103delinsCTG	XP_011527365.1:p.Ser34=
XM_011529064.2:c.101_103delinsCTG	XP_011527366.1:p.Ser34=
XM_011529065.2:c.101_103delinsCTG	XP_011527367.1:p.Ser34=
XM_017028087.2:c.38_40delinsCTG	XP_016883576.1:p.Ser13=
XR_936641.2:n.224_226delinsCTG
NM_030777.4:c.38_40delinsCTG MANE Select	NP_110404.1:p.Ser13=