Canonical Allele Identifier: CA2366796998

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46727087T= , CM000682.2:g.46727087T=	GRCh38
NC_000020.10:g.45355726T= , CM000682.1:g.45355726T=	GRCh37
NC_000020.9:g.44789133T=	NCBI36
NG_016284.1:g.22448T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1411+101T= MANE Select	ENSP00000352216.2:n.1411+101T=
ENST00000359271.3:c.1411+101T=	ENSP00000352216.2:n.1411+101T=
NM_030777.3:c.1411+101T=	NP_110404.1:n.1411+101T=
XM_011529060.1:c.1474+101T=	XP_011527362.1:n.1474+101T=
XM_011529061.1:c.1420+101T=	XP_011527363.1:n.1420+101T=
XM_011529062.1:c.1523+101T=	XP_011527364.1:n.1523+101T=
XM_011529063.1:c.1474+101T=	XP_011527365.1:n.1474+101T=
XM_011529064.1:c.1523+101T=	XP_011527366.1:n.1523+101T=
XM_011529065.1:c.1474+101T=	XP_011527367.1:n.1474+101T=
XR_936641.1:n.1659+101T=
XM_011529060.2:c.1474+101T=	XP_011527362.1:n.1474+101T=
XM_011529061.2:c.1420+101T=	XP_011527363.1:n.1420+101T=
XM_011529062.2:c.1523+101T=	XP_011527364.1:n.1523+101T=
XM_011529063.2:c.1474+101T=	XP_011527365.1:n.1474+101T=
XM_011529064.2:c.1523+101T=	XP_011527366.1:n.1523+101T=
XM_011529065.2:c.1474+101T=	XP_011527367.1:n.1474+101T=
XM_017028087.2:c.1411+101T=	XP_016883576.1:n.1411+101T=
XR_936641.2:n.1646+101T=
NM_030777.4:c.1411+101T= MANE Select	NP_110404.1:n.1411+101T=