Canonical Allele Identifier: CA913184880
Gene: SLC2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16112
dbSNP Id: rs2124448824

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929615_42929626del , CM000663.2:g.42929615_42929626del GRCh38
NC_000001.10:g.43395286_43395297del , CM000663.1:g.43395286_43395297del GRCh37
NC_000001.9:g.43167873_43167884del NCBI36
NG_008232.1:g.34560_34571del

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.843_854del MANE Select ENSP00000416293.2:p.Gln282_Ser285del
ENST00000674765.1:c.843_854del ENSP00000501811.1:p.Gln282_Ser285del
ENST00000675112.1:n.866_877del
ENST00000676254.1:n.1292_1303del
ENST00000426263.7:c.843_854del ENSP00000416293.2:p.Gln282_Ser285del
ENST00000439722.2:c.722_733del ENSP00000395521.2:n.722_733del
ENST00000475162.3:c.415+1009_415+1020del
ENST00000630287.2:c.*158_*169del ENSP00000486694.1:n.*158_*169del
NM_006516.2:c.843_854del NP_006507.2:p.Gln282_Ser285del
NM_006516.3:c.843_854del NP_006507.2:p.Gln282_Ser285del
NM_006516.4:c.843_854del MANE Select NP_006507.2:p.Gln282_Ser285del