Canonical Allele Identifier: CA2366796046

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725126A= , CM000682.2:g.46725126A=	GRCh38
NC_000020.10:g.45353765A= , CM000682.1:g.45353765A=	GRCh37
NC_000020.9:g.44787172A=	NCBI36
NG_016284.1:g.20487A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.90A= MANE Select	ENSP00000352216.2:p.Ser30=
ENST00000359271.3:c.90A=	ENSP00000352216.2:p.Ser30=
ENST00000611837.1:n.242A=
NM_030777.3:c.90A=	NP_110404.1:p.Ser30=
XM_011529060.1:c.153A=	XP_011527362.1:p.Ser51=
XM_011529061.1:c.99A=	XP_011527363.1:p.Ser33=
XM_011529062.1:c.153A=	XP_011527364.1:p.Ser51=
XM_011529063.1:c.153A=	XP_011527365.1:p.Ser51=
XM_011529064.1:c.153A=	XP_011527366.1:p.Ser51=
XM_011529065.1:c.153A=	XP_011527367.1:p.Ser51=
XR_936641.1:n.289A=
XM_011529060.2:c.153A=	XP_011527362.1:p.Ser51=
XM_011529061.2:c.99A=	XP_011527363.1:p.Ser33=
XM_011529062.2:c.153A=	XP_011527364.1:p.Ser51=
XM_011529063.2:c.153A=	XP_011527365.1:p.Ser51=
XM_011529064.2:c.153A=	XP_011527366.1:p.Ser51=
XM_011529065.2:c.153A=	XP_011527367.1:p.Ser51=
XM_017028087.2:c.90A=	XP_016883576.1:p.Ser30=
XR_936641.2:n.276A=
NM_030777.4:c.90A= MANE Select	NP_110404.1:p.Ser30=