Canonical Allele Identifier: CA9891979
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs777304011

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725507G>A , CM000682.2:g.46725507G>A GRCh38
NC_000020.10:g.45354146G>A , CM000682.1:g.45354146G>A GRCh37
NC_000020.9:g.44787553G>A NCBI36
NG_016284.1:g.20868G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.471G>A MANE Select ENSP00000352216.2:p.Leu157=
ENST00000359271.3:c.471G>A ENSP00000352216.2:p.Leu157=
NM_030777.3:c.471G>A NP_110404.1:p.Leu157=
XM_011529060.1:c.534G>A XP_011527362.1:p.Leu178=
XM_011529061.1:c.480G>A XP_011527363.1:p.Leu160=
XM_011529062.1:c.534G>A XP_011527364.1:p.Leu178=
XM_011529063.1:c.534G>A XP_011527365.1:p.Leu178=
XM_011529064.1:c.534G>A XP_011527366.1:p.Leu178=
XM_011529065.1:c.534G>A XP_011527367.1:p.Leu178=
XR_936641.1:n.670G>A
XM_011529060.2:c.534G>A XP_011527362.1:p.Leu178=
XM_011529061.2:c.480G>A XP_011527363.1:p.Leu160=
XM_011529062.2:c.534G>A XP_011527364.1:p.Leu178=
XM_011529063.2:c.534G>A XP_011527365.1:p.Leu178=
XM_011529064.2:c.534G>A XP_011527366.1:p.Leu178=
XM_011529065.2:c.534G>A XP_011527367.1:p.Leu178=
XM_017028087.2:c.471G>A XP_016883576.1:p.Leu157=
XR_936641.2:n.657G>A
NM_030777.4:c.471G>A MANE Select NP_110404.1:p.Leu157=