Canonical Allele Identifier: CA1165412468
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929976G= , CM000663.2:g.42929976G= GRCh38
NC_000001.10:g.43395647G= , CM000663.1:g.43395647G= GRCh37
NC_000001.9:g.43168234G= NCBI36
NG_008232.1:g.34201C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.576C= MANE Select ENSP00000416293.2:p.Ile192=
ENST00000674765.1:c.576C= ENSP00000501811.1:p.Ile192=
ENST00000675112.1:n.599C=
ENST00000676254.1:n.1025C=
ENST00000426263.7:c.576C= ENSP00000416293.2:p.Ile192=
ENST00000439722.2:c.455C= ENSP00000395521.2:n.455C=
ENST00000475162.3:c.415+650C=
ENST00000630287.2:c.517-196C= ENSP00000486694.1:n.517-196C=
NM_006516.2:c.576C= NP_006507.2:p.Ile192=
NM_006516.3:c.576C= NP_006507.2:p.Ile192=
NM_006516.4:c.576C= MANE Select NP_006507.2:p.Ile192=