Canonical Allele Identifier: CA9892140

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726326T>C , CM000682.2:g.46726326T>C	GRCh38
NC_000020.10:g.45354965T>C , CM000682.1:g.45354965T>C	GRCh37
NC_000020.9:g.44788372T>C	NCBI36
NG_016284.1:g.21687T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.1288+2T>C MANE Select	NP_110404.1:n.1288+2T>C
ENST00000359271.4:c.1288+2T>C MANE Select	ENSP00000352216.2:n.1288+2T>C
NM_030777.3:c.1288+2T>C	NP_110404.1:n.1288+2T>C
ENST00000359271.3:c.1288+2T>C	ENSP00000352216.2:n.1288+2T>C
XM_011529060.1:c.1351+2T>C	XP_011527362.1:n.1351+2T>C
XM_011529060.2:c.1351+2T>C	XP_011527362.1:n.1351+2T>C
XM_011529061.1:c.1297+2T>C	XP_011527363.1:n.1297+2T>C
XM_011529061.2:c.1297+2T>C	XP_011527363.1:n.1297+2T>C
XM_011529062.1:c.1351+2T>C	XP_011527364.1:n.1351+2T>C
XM_011529062.2:c.1351+2T>C	XP_011527364.1:n.1351+2T>C
XM_011529063.1:c.1351+2T>C	XP_011527365.1:n.1351+2T>C
XM_011529063.2:c.1351+2T>C	XP_011527365.1:n.1351+2T>C
XM_011529064.1:c.1351+2T>C	XP_011527366.1:n.1351+2T>C
XM_011529064.2:c.1351+2T>C	XP_011527366.1:n.1351+2T>C
XM_011529065.1:c.1351+2T>C	XP_011527367.1:n.1351+2T>C
XM_011529065.2:c.1351+2T>C	XP_011527367.1:n.1351+2T>C
XM_017028087.2:c.1288+2T>C	XP_016883576.1:n.1288+2T>C
XR_936641.1:n.1487+2T>C
XR_936641.2:n.1474+2T>C