Canonical Allele Identifier: CA2366796134

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725308C= , CM000682.2:g.46725308C=	GRCh38
NC_000020.10:g.45353947C= , CM000682.1:g.45353947C=	GRCh37
NC_000020.9:g.44787354C=	NCBI36
NG_016284.1:g.20669C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.272C= MANE Select	ENSP00000352216.2:p.Thr91=
ENST00000359271.3:c.272C=	ENSP00000352216.2:p.Thr91=
ENST00000611837.1:n.424C=
NM_030777.3:c.272C=	NP_110404.1:p.Thr91=
XM_011529060.1:c.335C=	XP_011527362.1:p.Thr112=
XM_011529061.1:c.281C=	XP_011527363.1:p.Thr94=
XM_011529062.1:c.335C=	XP_011527364.1:p.Thr112=
XM_011529063.1:c.335C=	XP_011527365.1:p.Thr112=
XM_011529064.1:c.335C=	XP_011527366.1:p.Thr112=
XM_011529065.1:c.335C=	XP_011527367.1:p.Thr112=
XR_936641.1:n.471C=
XM_011529060.2:c.335C=	XP_011527362.1:p.Thr112=
XM_011529061.2:c.281C=	XP_011527363.1:p.Thr94=
XM_011529062.2:c.335C=	XP_011527364.1:p.Thr112=
XM_011529063.2:c.335C=	XP_011527365.1:p.Thr112=
XM_011529064.2:c.335C=	XP_011527366.1:p.Thr112=
XM_011529065.2:c.335C=	XP_011527367.1:p.Thr112=
XM_017028087.2:c.272C=	XP_016883576.1:p.Thr91=
XR_936641.2:n.458C=
NM_030777.4:c.272C= MANE Select	NP_110404.1:p.Thr91=