Canonical Allele Identifier: CA744919093

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1276012380
• MyVariant Identifiers: chr20:g.45353487_45353494del (hg19) ; chr20:g.46724848_46724855del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724849_46724856del , CM000682.2:g.46724849_46724856del	GRCh38
NC_000020.10:g.45353488_45353495del , CM000682.1:g.45353488_45353495del	GRCh37
NC_000020.9:g.44786895_44786902del	NCBI36
NG_016284.1:g.20210_20217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-192_5-185del MANE Select	ENSP00000352216.2:n.5-192_5-185del
ENST00000359271.3:c.5-192_5-185del	ENSP00000352216.2:n.5-192_5-185del
ENST00000611837.1:n.157-192_157-185del
NM_030777.3:c.5-192_5-185del	NP_110404.1:n.5-192_5-185del
XM_011529060.1:c.68-192_68-185del	XP_011527362.1:n.68-192_68-185del
XM_011529061.1:c.14-192_14-185del	XP_011527363.1:n.14-192_14-185del
XM_011529062.1:c.68-192_68-185del	XP_011527364.1:n.68-192_68-185del
XM_011529063.1:c.68-192_68-185del	XP_011527365.1:n.68-192_68-185del
XM_011529064.1:c.68-192_68-185del	XP_011527366.1:n.68-192_68-185del
XM_011529065.1:c.68-192_68-185del	XP_011527367.1:n.68-192_68-185del
XR_936641.1:n.204-192_204-185del
XM_011529060.2:c.68-192_68-185del	XP_011527362.1:n.68-192_68-185del
XM_011529061.2:c.14-192_14-185del	XP_011527363.1:n.14-192_14-185del
XM_011529062.2:c.68-192_68-185del	XP_011527364.1:n.68-192_68-185del
XM_011529063.2:c.68-192_68-185del	XP_011527365.1:n.68-192_68-185del
XM_011529064.2:c.68-192_68-185del	XP_011527366.1:n.68-192_68-185del
XM_011529065.2:c.68-192_68-185del	XP_011527367.1:n.68-192_68-185del
XM_017028087.2:c.5-192_5-185del	XP_016883576.1:n.5-192_5-185del
XR_936641.2:n.191-192_191-185del
NM_030777.4:c.5-192_5-185del MANE Select	NP_110404.1:n.5-192_5-185del