Canonical Allele Identifier: CA744919179

Gene: SLC2A10

Linked Data

• dbSNP Id: rs139655963
• MyVariant Identifiers: chr20:g.45353514_45353515insAGAT (hg19) ; chr20:g.46724875_46724876insAGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724875_46724876insAGAT , CM000682.2:g.46724875_46724876insAGAT	GRCh38
NC_000020.10:g.45353514_45353515insAGAT , CM000682.1:g.45353514_45353515insAGAT	GRCh37
NC_000020.9:g.44786921_44786922insAGAT	NCBI36
NG_016284.1:g.20236_20237insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-166_5-165insAGAT MANE Select	ENSP00000352216.2:n.5-166_5-165insAGAT
ENST00000359271.3:c.5-166_5-165insAGAT	ENSP00000352216.2:n.5-166_5-165insAGAT
ENST00000611837.1:n.157-166_157-165insAGAT
NM_030777.3:c.5-166_5-165insAGAT	NP_110404.1:n.5-166_5-165insAGAT
XM_011529060.1:c.68-166_68-165insAGAT	XP_011527362.1:n.68-166_68-165insAGAT
XM_011529061.1:c.14-166_14-165insAGAT	XP_011527363.1:n.14-166_14-165insAGAT
XM_011529062.1:c.68-166_68-165insAGAT	XP_011527364.1:n.68-166_68-165insAGAT
XM_011529063.1:c.68-166_68-165insAGAT	XP_011527365.1:n.68-166_68-165insAGAT
XM_011529064.1:c.68-166_68-165insAGAT	XP_011527366.1:n.68-166_68-165insAGAT
XM_011529065.1:c.68-166_68-165insAGAT	XP_011527367.1:n.68-166_68-165insAGAT
XR_936641.1:n.204-166_204-165insAGAT
XM_011529060.2:c.68-166_68-165insAGAT	XP_011527362.1:n.68-166_68-165insAGAT
XM_011529061.2:c.14-166_14-165insAGAT	XP_011527363.1:n.14-166_14-165insAGAT
XM_011529062.2:c.68-166_68-165insAGAT	XP_011527364.1:n.68-166_68-165insAGAT
XM_011529063.2:c.68-166_68-165insAGAT	XP_011527365.1:n.68-166_68-165insAGAT
XM_011529064.2:c.68-166_68-165insAGAT	XP_011527366.1:n.68-166_68-165insAGAT
XM_011529065.2:c.68-166_68-165insAGAT	XP_011527367.1:n.68-166_68-165insAGAT
XM_017028087.2:c.5-166_5-165insAGAT	XP_016883576.1:n.5-166_5-165insAGAT
XR_936641.2:n.191-166_191-165insAGAT
NM_030777.4:c.5-166_5-165insAGAT MANE Select	NP_110404.1:n.5-166_5-165insAGAT