Canonical Allele Identifier: CA1165412736
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930638G= , CM000663.2:g.42930638G= GRCh38
NC_000001.10:g.43396309G= , CM000663.1:g.43396309G= GRCh37
NC_000001.9:g.43168896G= NCBI36
NG_008232.1:g.33539C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.504C= MANE Select ENSP00000416293.2:p.Ile168=
ENST00000674765.1:c.504C= ENSP00000501811.1:p.Ile168=
ENST00000675112.1:n.527C=
ENST00000676254.1:n.953C=
ENST00000426263.7:c.504C= ENSP00000416293.2:p.Ile168=
ENST00000439722.2:c.383C= ENSP00000395521.2:n.383C=
ENST00000475162.3:c.403C=
ENST00000625233.2:n.712C=
ENST00000630287.2:c.504C= ENSP00000486694.1:p.Ile168=
NM_006516.2:c.504C= NP_006507.2:p.Ile168=
NM_006516.3:c.504C= NP_006507.2:p.Ile168=
NM_006516.4:c.504C= MANE Select NP_006507.2:p.Ile168=