Canonical Allele Identifier: CA1142031352
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929634C= , CM000663.2:g.42929634C= GRCh38
NC_000001.10:g.43395305C= , CM000663.1:g.43395305C= GRCh37
NC_000001.9:g.43167892C= NCBI36
NG_008232.1:g.34543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.826G= MANE Select ENSP00000416293.2:p.Val276=
ENST00000674765.1:c.826G= ENSP00000501811.1:p.Val276=
ENST00000675112.1:n.849G=
ENST00000676254.1:n.1275G=
ENST00000426263.7:c.826G= ENSP00000416293.2:p.Val276=
ENST00000439722.2:c.705G= ENSP00000395521.2:n.705G=
ENST00000475162.3:c.415+992G=
ENST00000630287.2:c.*141G= ENSP00000486694.1:n.*141G=
NM_006516.2:c.826G= NP_006507.2:p.Val276=
NM_006516.3:c.826G= NP_006507.2:p.Val276=
NM_006516.4:c.826G= MANE Select NP_006507.2:p.Val276=