Canonical Allele Identifier: CA510847486

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 2721545
• ClinVar RCV Id: RCV003504130
• MyVariant Identifiers: chr20:g.45353921C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725282C>T , CM000682.2:g.46725282C>T	GRCh38
NC_000020.10:g.45353921C>T , CM000682.1:g.45353921C>T	GRCh37
NC_000020.9:g.44787328C>T	NCBI36
NG_016284.1:g.20643C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.246C>T MANE Select	ENSP00000352216.2:p.Asn82=
ENST00000359271.3:c.246C>T	ENSP00000352216.2:p.Asn82=
ENST00000611837.1:n.398C>T
NM_030777.3:c.246C>T	NP_110404.1:p.Asn82=
XM_011529060.1:c.309C>T	XP_011527362.1:p.Asn103=
XM_011529061.1:c.255C>T	XP_011527363.1:p.Asn85=
XM_011529062.1:c.309C>T	XP_011527364.1:p.Asn103=
XM_011529063.1:c.309C>T	XP_011527365.1:p.Asn103=
XM_011529064.1:c.309C>T	XP_011527366.1:p.Asn103=
XM_011529065.1:c.309C>T	XP_011527367.1:p.Asn103=
XR_936641.1:n.445C>T
XM_011529060.2:c.309C>T	XP_011527362.1:p.Asn103=
XM_011529061.2:c.255C>T	XP_011527363.1:p.Asn85=
XM_011529062.2:c.309C>T	XP_011527364.1:p.Asn103=
XM_011529063.2:c.309C>T	XP_011527365.1:p.Asn103=
XM_011529064.2:c.309C>T	XP_011527366.1:p.Asn103=
XM_011529065.2:c.309C>T	XP_011527367.1:p.Asn103=
XM_017028087.2:c.246C>T	XP_016883576.1:p.Asn82=
XR_936641.2:n.432C>T
NM_030777.4:c.246C>T MANE Select	NP_110404.1:p.Asn82=