Canonical Allele Identifier: CA510770873

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45353762A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725123A>C , CM000682.2:g.46725123A>C	GRCh38
NC_000020.10:g.45353762A>C , CM000682.1:g.45353762A>C	GRCh37
NC_000020.9:g.44787169A>C	NCBI36
NG_016284.1:g.20484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.87A>C MANE Select	ENSP00000352216.2:p.Ile29=
ENST00000359271.3:c.87A>C	ENSP00000352216.2:p.Ile29=
ENST00000611837.1:n.239A>C
NM_030777.3:c.87A>C	NP_110404.1:p.Ile29=
XM_011529060.1:c.150A>C	XP_011527362.1:p.Ile50=
XM_011529061.1:c.96A>C	XP_011527363.1:p.Ile32=
XM_011529062.1:c.150A>C	XP_011527364.1:p.Ile50=
XM_011529063.1:c.150A>C	XP_011527365.1:p.Ile50=
XM_011529064.1:c.150A>C	XP_011527366.1:p.Ile50=
XM_011529065.1:c.150A>C	XP_011527367.1:p.Ile50=
XR_936641.1:n.286A>C
XM_011529060.2:c.150A>C	XP_011527362.1:p.Ile50=
XM_011529061.2:c.96A>C	XP_011527363.1:p.Ile32=
XM_011529062.2:c.150A>C	XP_011527364.1:p.Ile50=
XM_011529063.2:c.150A>C	XP_011527365.1:p.Ile50=
XM_011529064.2:c.150A>C	XP_011527366.1:p.Ile50=
XM_011529065.2:c.150A>C	XP_011527367.1:p.Ile50=
XM_017028087.2:c.87A>C	XP_016883576.1:p.Ile29=
XR_936641.2:n.273A>C
NM_030777.4:c.87A>C MANE Select	NP_110404.1:p.Ile29=