Canonical Allele Identifier: CA293565

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46733825G>A , CM000682.2:g.46733825G>A	GRCh38
NC_000020.10:g.45362464G>A , CM000682.1:g.45362464G>A	GRCh37
NC_000020.9:g.44795871G>A	NCBI36
NG_016284.1:g.29186G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1617G>A MANE Select	ENSP00000352216.2:p.Ala539=
ENST00000359271.3:c.1617G>A	ENSP00000352216.2:p.Ala539=
NM_030777.3:c.1617G>A	NP_110404.1:p.Ala539=
XM_011529060.1:c.1680G>A	XP_011527362.1:p.Ala560=
XM_011529061.1:c.1626G>A	XP_011527363.1:p.Ala542=
XM_011529062.1:c.1593G>A	XP_011527364.1:p.Ala531=
XM_011529065.1:c.*59G>A	XP_011527367.1:n.*59G>A
XR_936641.1:n.1865G>A
XM_011529060.2:c.1680G>A	XP_011527362.1:p.Ala560=
XM_011529061.2:c.1626G>A	XP_011527363.1:p.Ala542=
XM_011529062.2:c.1593G>A	XP_011527364.1:p.Ala531=
XM_011529065.2:c.*59G>A	XP_011527367.1:n.*59G>A
XM_017028087.2:c.*59G>A	XP_016883576.1:n.*59G>A
XR_936641.2:n.1852G>A
NM_030777.4:c.1617G>A MANE Select	NP_110404.1:p.Ala539=