Canonical Allele Identifier: CA9892189

Gene: SLC2A10

Linked Data

• dbSNP Id: rs769654615
• ExAC: 20:45355649 G / GT
• gnomAD v2: 20-45355649-G-GT
• gnomAD v4: 20-46727010-G-GT
• MyVariant Identifiers: chr20:g.45355650_45355651insT (hg19) ; chr20:g.45355649_45355650insT (hg19) ; chr20:g.46727010_46727011insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46727018dup , CM000682.2:g.46727018dup	GRCh38
NC_000020.10:g.45355657dup , CM000682.1:g.45355657dup	GRCh37
NC_000020.9:g.44789064dup	NCBI36
NG_016284.1:g.22379dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1411+32dup MANE Select	ENSP00000352216.2:n.1411+32dup
ENST00000359271.3:c.1411+32dup	ENSP00000352216.2:n.1411+32dup
NM_030777.3:c.1411+32dup	NP_110404.1:n.1411+32dup
XM_011529060.1:c.1474+32dup	XP_011527362.1:n.1474+32dup
XM_011529061.1:c.1420+32dup	XP_011527363.1:n.1420+32dup
XM_011529062.1:c.1523+32dup	XP_011527364.1:n.1523+32dup
XM_011529063.1:c.1474+32dup	XP_011527365.1:n.1474+32dup
XM_011529064.1:c.1523+32dup	XP_011527366.1:n.1523+32dup
XM_011529065.1:c.1474+32dup	XP_011527367.1:n.1474+32dup
XR_936641.1:n.1659+32dup
XM_011529060.2:c.1474+32dup	XP_011527362.1:n.1474+32dup
XM_011529061.2:c.1420+32dup	XP_011527363.1:n.1420+32dup
XM_011529062.2:c.1523+32dup	XP_011527364.1:n.1523+32dup
XM_011529063.2:c.1474+32dup	XP_011527365.1:n.1474+32dup
XM_011529064.2:c.1523+32dup	XP_011527366.1:n.1523+32dup
XM_011529065.2:c.1474+32dup	XP_011527367.1:n.1474+32dup
XM_017028087.2:c.1411+32dup	XP_016883576.1:n.1411+32dup
XR_936641.2:n.1646+32dup
NM_030777.4:c.1411+32dup MANE Select	NP_110404.1:n.1411+32dup