Canonical Allele Identifier: CA1165412645
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930412G= , CM000663.2:g.42930412G= GRCh38
NC_000001.10:g.43396083G= , CM000663.1:g.43396083G= GRCh37
NC_000001.9:g.43168670G= NCBI36
NG_008232.1:g.33765C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.516+214C= MANE Select ENSP00000416293.2:n.516+214C=
ENST00000674765.1:c.516+214C= ENSP00000501811.1:n.516+214C=
ENST00000675112.1:n.539+214C=
ENST00000676254.1:n.965+214C=
ENST00000426263.7:c.516+214C= ENSP00000416293.2:n.516+214C=
ENST00000439722.2:c.395+214C= ENSP00000395521.2:n.395+214C=
ENST00000475162.3:c.415+214C=
ENST00000625233.2:n.938C=
ENST00000630287.2:c.516+214C= ENSP00000486694.1:n.516+214C=
NM_006516.2:c.516+214C= NP_006507.2:n.516+214C=
NM_006516.3:c.516+214C= NP_006507.2:n.516+214C=
NM_006516.4:c.516+214C= MANE Select NP_006507.2:n.516+214C=