Canonical Allele Identifier: CA2366796955

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46727002A= , CM000682.2:g.46727002A=	GRCh38
NC_000020.10:g.45355641A= , CM000682.1:g.45355641A=	GRCh37
NC_000020.9:g.44789048A=	NCBI36
NG_016284.1:g.22363A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1411+16A= MANE Select	ENSP00000352216.2:n.1411+16A=
ENST00000359271.3:c.1411+16A=	ENSP00000352216.2:n.1411+16A=
NM_030777.3:c.1411+16A=	NP_110404.1:n.1411+16A=
XM_011529060.1:c.1474+16A=	XP_011527362.1:n.1474+16A=
XM_011529061.1:c.1420+16A=	XP_011527363.1:n.1420+16A=
XM_011529062.1:c.1523+16A=	XP_011527364.1:n.1523+16A=
XM_011529063.1:c.1474+16A=	XP_011527365.1:n.1474+16A=
XM_011529064.1:c.1523+16A=	XP_011527366.1:n.1523+16A=
XM_011529065.1:c.1474+16A=	XP_011527367.1:n.1474+16A=
XR_936641.1:n.1659+16A=
XM_011529060.2:c.1474+16A=	XP_011527362.1:n.1474+16A=
XM_011529061.2:c.1420+16A=	XP_011527363.1:n.1420+16A=
XM_011529062.2:c.1523+16A=	XP_011527364.1:n.1523+16A=
XM_011529063.2:c.1474+16A=	XP_011527365.1:n.1474+16A=
XM_011529064.2:c.1523+16A=	XP_011527366.1:n.1523+16A=
XM_011529065.2:c.1474+16A=	XP_011527367.1:n.1474+16A=
XM_017028087.2:c.1411+16A=	XP_016883576.1:n.1411+16A=
XR_936641.2:n.1646+16A=
NM_030777.4:c.1411+16A= MANE Select	NP_110404.1:n.1411+16A=