Canonical Allele Identifier: CA315754775

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1555887727
• MyVariant Identifiers: chr20:g.45353479_45353480insATGGTTTGA (hg19) ; chr20:g.46724840_46724841insATGGTTTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724844_46724845insTTTGAATGG , CM000682.2:g.46724844_46724845insTTTGAATGG	GRCh38
NC_000020.10:g.45353483_45353484insTTTGAATGG , CM000682.1:g.45353483_45353484insTTTGAATGG	GRCh37
NC_000020.9:g.44786890_44786891insTTTGAATGG	NCBI36
NG_016284.1:g.20205_20206insTTTGAATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-197_5-196insTTTGAATGG MANE Select	ENSP00000352216.2:n.5-197_5-196insTTTGAATGG
ENST00000359271.3:c.5-197_5-196insTTTGAATGG	ENSP00000352216.2:n.5-197_5-196insTTTGAATGG
ENST00000611837.1:n.157-197_157-196insTTTGAATGG
NM_030777.3:c.5-197_5-196insTTTGAATGG	NP_110404.1:n.5-197_5-196insTTTGAATGG
XM_011529060.1:c.68-197_68-196insTTTGAATGG	XP_011527362.1:n.68-197_68-196insTTTGAATGG
XM_011529061.1:c.14-197_14-196insTTTGAATGG	XP_011527363.1:n.14-197_14-196insTTTGAATGG
XM_011529062.1:c.68-197_68-196insTTTGAATGG	XP_011527364.1:n.68-197_68-196insTTTGAATGG
XM_011529063.1:c.68-197_68-196insTTTGAATGG	XP_011527365.1:n.68-197_68-196insTTTGAATGG
XM_011529064.1:c.68-197_68-196insTTTGAATGG	XP_011527366.1:n.68-197_68-196insTTTGAATGG
XM_011529065.1:c.68-197_68-196insTTTGAATGG	XP_011527367.1:n.68-197_68-196insTTTGAATGG
XR_936641.1:n.204-197_204-196insTTTGAATGG
XM_011529060.2:c.68-197_68-196insTTTGAATGG	XP_011527362.1:n.68-197_68-196insTTTGAATGG
XM_011529061.2:c.14-197_14-196insTTTGAATGG	XP_011527363.1:n.14-197_14-196insTTTGAATGG
XM_011529062.2:c.68-197_68-196insTTTGAATGG	XP_011527364.1:n.68-197_68-196insTTTGAATGG
XM_011529063.2:c.68-197_68-196insTTTGAATGG	XP_011527365.1:n.68-197_68-196insTTTGAATGG
XM_011529064.2:c.68-197_68-196insTTTGAATGG	XP_011527366.1:n.68-197_68-196insTTTGAATGG
XM_011529065.2:c.68-197_68-196insTTTGAATGG	XP_011527367.1:n.68-197_68-196insTTTGAATGG
XM_017028087.2:c.5-197_5-196insTTTGAATGG	XP_016883576.1:n.5-197_5-196insTTTGAATGG
XR_936641.2:n.191-197_191-196insTTTGAATGG
NM_030777.4:c.5-197_5-196insTTTGAATGG MANE Select	NP_110404.1:n.5-197_5-196insTTTGAATGG