Canonical Allele Identifier: CA1165411579
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927806C= , CM000663.2:g.42927806C= GRCh38
NC_000001.10:g.43393477C= , CM000663.1:g.43393477C= GRCh37
NC_000001.9:g.43166064C= NCBI36
NG_008232.1:g.36371G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1077G= MANE Select ENSP00000416293.2:p.Glu359=
ENST00000674545.1:n.1694G=
ENST00000674765.1:c.1030-949G= ENSP00000501811.1:n.1030-949G=
ENST00000675112.1:n.1378G=
ENST00000676254.1:n.1526G=
ENST00000426263.7:c.1077G= ENSP00000416293.2:p.Glu359=
ENST00000475162.3:c.416-828G=
ENST00000630287.2:c.*392G= ENSP00000486694.1:n.*392G=
NM_006516.2:c.1077G= NP_006507.2:p.Glu359=
NM_006516.3:c.1077G= NP_006507.2:p.Glu359=
NM_006516.4:c.1077G= MANE Select NP_006507.2:p.Glu359=