Canonical Allele Identifier: CA2560576181
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725500_46725501insCG , CM000682.2:g.46725500_46725501insCG GRCh38
NC_000020.10:g.45354139_45354140insCG , CM000682.1:g.45354139_45354140insCG GRCh37
NC_000020.9:g.44787546_44787547insCG NCBI36
NG_016284.1:g.20861_20862insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.464_465insCG MANE Select ENSP00000352216.2:p.Ala156ValfsTer?
ENST00000359271.3:c.464_465insCG ENSP00000352216.2:p.Ala156ValfsTer?
NM_030777.3:c.464_465insCG NP_110404.1:p.Ala156ValfsTer?
XM_011529060.1:c.527_528insCG XP_011527362.1:p.Ala177ValfsTer?
XM_011529061.1:c.473_474insCG XP_011527363.1:p.Ala159ValfsTer?
XM_011529062.1:c.527_528insCG XP_011527364.1:p.Ala177ValfsTer?
XM_011529063.1:c.527_528insCG XP_011527365.1:p.Ala177ValfsTer?
XM_011529064.1:c.527_528insCG XP_011527366.1:p.Ala177ValfsTer?
XM_011529065.1:c.527_528insCG XP_011527367.1:p.Ala177ValfsTer?
XR_936641.1:n.663_664insCG
XM_011529060.2:c.527_528insCG XP_011527362.1:p.Ala177ValfsTer?
XM_011529061.2:c.473_474insCG XP_011527363.1:p.Ala159ValfsTer?
XM_011529062.2:c.527_528insCG XP_011527364.1:p.Ala177ValfsTer?
XM_011529063.2:c.527_528insCG XP_011527365.1:p.Ala177ValfsTer?
XM_011529064.2:c.527_528insCG XP_011527366.1:p.Ala177ValfsTer?
XM_011529065.2:c.527_528insCG XP_011527367.1:p.Ala177ValfsTer?
XM_017028087.2:c.464_465insCG XP_016883576.1:p.Ala156ValfsTer?
XR_936641.2:n.650_651insCG
NM_030777.4:c.464_465insCG MANE Select NP_110404.1:p.Ala156ValfsTer?