Canonical Allele Identifier: CA1165412183
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929243G= , CM000663.2:g.42929243G= GRCh38
NC_000001.10:g.43394914G= , CM000663.1:g.43394914G= GRCh37
NC_000001.9:g.43167501G= NCBI36
NG_008232.1:g.34934C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.939C= MANE Select ENSP00000416293.2:p.Ser313=
ENST00000674545.1:n.257C=
ENST00000674765.1:c.939C= ENSP00000501811.1:p.Ser313=
ENST00000675112.1:n.1240C=
ENST00000676254.1:n.1388C=
ENST00000426263.7:c.939C= ENSP00000416293.2:p.Ser313=
ENST00000439722.2:c.818C= ENSP00000395521.2:n.818C=
ENST00000475162.3:c.415+1383C=
ENST00000630287.2:c.*254C= ENSP00000486694.1:n.*254C=
NM_006516.2:c.939C= NP_006507.2:p.Ser313=
NM_006516.3:c.939C= NP_006507.2:p.Ser313=
NM_006516.4:c.939C= MANE Select NP_006507.2:p.Ser313=