Canonical Allele Identifier: CA636057091

Gene: SLC2A10

Linked Data

• dbSNP Id: rs111504264
• gnomAD v2: 20-45353445-AGGATGGAT-A
• gnomAD v3: 20-46724806-AGGATGGAT-A
• gnomAD v4: 20-46724806-AGGATGGAT-A
• MyVariant Identifiers: chr20:g.45353450_45353457del (hg19) ; chr20:g.45353446_45353453del (hg19) ; chr20:g.46724811_46724818del (hg38) ; chr20:g.46724807_46724814del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724841_46724848del , CM000682.2:g.46724841_46724848del	GRCh38
NC_000020.10:g.45353480_45353487del , CM000682.1:g.45353480_45353487del	GRCh37
NC_000020.9:g.44786887_44786894del	NCBI36
NG_016284.1:g.20202_20209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-200_5-193del MANE Select	ENSP00000352216.2:n.5-200_5-193del
ENST00000359271.3:c.5-200_5-193del	ENSP00000352216.2:n.5-200_5-193del
ENST00000611837.1:n.157-200_157-193del
NM_030777.3:c.5-200_5-193del	NP_110404.1:n.5-200_5-193del
XM_011529060.1:c.68-200_68-193del	XP_011527362.1:n.68-200_68-193del
XM_011529061.1:c.14-200_14-193del	XP_011527363.1:n.14-200_14-193del
XM_011529062.1:c.68-200_68-193del	XP_011527364.1:n.68-200_68-193del
XM_011529063.1:c.68-200_68-193del	XP_011527365.1:n.68-200_68-193del
XM_011529064.1:c.68-200_68-193del	XP_011527366.1:n.68-200_68-193del
XM_011529065.1:c.68-200_68-193del	XP_011527367.1:n.68-200_68-193del
XR_936641.1:n.204-200_204-193del
XM_011529060.2:c.68-200_68-193del	XP_011527362.1:n.68-200_68-193del
XM_011529061.2:c.14-200_14-193del	XP_011527363.1:n.14-200_14-193del
XM_011529062.2:c.68-200_68-193del	XP_011527364.1:n.68-200_68-193del
XM_011529063.2:c.68-200_68-193del	XP_011527365.1:n.68-200_68-193del
XM_011529064.2:c.68-200_68-193del	XP_011527366.1:n.68-200_68-193del
XM_011529065.2:c.68-200_68-193del	XP_011527367.1:n.68-200_68-193del
XM_017028087.2:c.5-200_5-193del	XP_016883576.1:n.5-200_5-193del
XR_936641.2:n.191-200_191-193del
NM_030777.4:c.5-200_5-193del MANE Select	NP_110404.1:n.5-200_5-193del