Canonical Allele Identifier: CA1165411566
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927777A= , CM000663.2:g.42927777A= GRCh38
NC_000001.10:g.43393448A= , CM000663.1:g.43393448A= GRCh37
NC_000001.9:g.43166035A= NCBI36
NG_008232.1:g.36400T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1106T= MANE Select ENSP00000416293.2:p.Ile369=
ENST00000674545.1:n.1723T=
ENST00000674765.1:c.1030-920T= ENSP00000501811.1:n.1030-920T=
ENST00000675112.1:n.1407T=
ENST00000676254.1:n.1555T=
ENST00000426263.7:c.1106T= ENSP00000416293.2:p.Ile369=
ENST00000475162.3:c.416-799T=
ENST00000630287.2:c.*421T= ENSP00000486694.1:n.*421T=
NM_006516.2:c.1106T= NP_006507.2:p.Ile369=
NM_006516.3:c.1106T= NP_006507.2:p.Ile369=
NM_006516.4:c.1106T= MANE Select NP_006507.2:p.Ile369=