Canonical Allele Identifier: CA510847779

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45354308G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725669G>C , CM000682.2:g.46725669G>C	GRCh38
NC_000020.10:g.45354308G>C , CM000682.1:g.45354308G>C	GRCh37
NC_000020.9:g.44787715G>C	NCBI36
NG_016284.1:g.21030G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.633G>C MANE Select	ENSP00000352216.2:p.Pro211=
ENST00000359271.3:c.633G>C	ENSP00000352216.2:p.Pro211=
NM_030777.3:c.633G>C	NP_110404.1:p.Pro211=
XM_011529060.1:c.696G>C	XP_011527362.1:p.Pro232=
XM_011529061.1:c.642G>C	XP_011527363.1:p.Pro214=
XM_011529062.1:c.696G>C	XP_011527364.1:p.Pro232=
XM_011529063.1:c.696G>C	XP_011527365.1:p.Pro232=
XM_011529064.1:c.696G>C	XP_011527366.1:p.Pro232=
XM_011529065.1:c.696G>C	XP_011527367.1:p.Pro232=
XR_936641.1:n.832G>C
XM_011529060.2:c.696G>C	XP_011527362.1:p.Pro232=
XM_011529061.2:c.642G>C	XP_011527363.1:p.Pro214=
XM_011529062.2:c.696G>C	XP_011527364.1:p.Pro232=
XM_011529063.2:c.696G>C	XP_011527365.1:p.Pro232=
XM_011529064.2:c.696G>C	XP_011527366.1:p.Pro232=
XM_011529065.2:c.696G>C	XP_011527367.1:p.Pro232=
XM_017028087.2:c.633G>C	XP_016883576.1:p.Pro211=
XR_936641.2:n.819G>C
NM_030777.4:c.633G>C MANE Select	NP_110404.1:p.Pro211=