Canonical Allele Identifier: CA315755159

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1014009929
• gnomAD v4: 20-46725177-G-A
• MyVariant Identifiers: chr20:g.45353816G>A (hg19) ; chr20:g.46725177G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725177G>A , CM000682.2:g.46725177G>A	GRCh38
NC_000020.10:g.45353816G>A , CM000682.1:g.45353816G>A	GRCh37
NC_000020.9:g.44787223G>A	NCBI36
NG_016284.1:g.20538G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.141G>A MANE Select	ENSP00000352216.2:p.Gln47=
ENST00000359271.3:c.141G>A	ENSP00000352216.2:p.Gln47=
ENST00000611837.1:n.293G>A
NM_030777.3:c.141G>A	NP_110404.1:p.Gln47=
XM_011529060.1:c.204G>A	XP_011527362.1:p.Gln68=
XM_011529061.1:c.150G>A	XP_011527363.1:p.Gln50=
XM_011529062.1:c.204G>A	XP_011527364.1:p.Gln68=
XM_011529063.1:c.204G>A	XP_011527365.1:p.Gln68=
XM_011529064.1:c.204G>A	XP_011527366.1:p.Gln68=
XM_011529065.1:c.204G>A	XP_011527367.1:p.Gln68=
XR_936641.1:n.340G>A
XM_011529060.2:c.204G>A	XP_011527362.1:p.Gln68=
XM_011529061.2:c.150G>A	XP_011527363.1:p.Gln50=
XM_011529062.2:c.204G>A	XP_011527364.1:p.Gln68=
XM_011529063.2:c.204G>A	XP_011527365.1:p.Gln68=
XM_011529064.2:c.204G>A	XP_011527366.1:p.Gln68=
XM_011529065.2:c.204G>A	XP_011527367.1:p.Gln68=
XM_017028087.2:c.141G>A	XP_016883576.1:p.Gln47=
XR_936641.2:n.327G>A
NM_030777.4:c.141G>A MANE Select	NP_110404.1:p.Gln47=