Canonical Allele Identifier: CA1148727536
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930632G= , CM000663.2:g.42930632G= GRCh38
NC_000001.10:g.43396303G= , CM000663.1:g.43396303G= GRCh37
NC_000001.9:g.43168890G= NCBI36
NG_008232.1:g.33545C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.510C= MANE Select ENSP00000416293.2:p.Ile170=
ENST00000674765.1:c.510C= ENSP00000501811.1:p.Ile170=
ENST00000675112.1:n.533C=
ENST00000676254.1:n.959C=
ENST00000426263.7:c.510C= ENSP00000416293.2:p.Ile170=
ENST00000439722.2:c.389C= ENSP00000395521.2:n.389C=
ENST00000475162.3:c.409C=
ENST00000625233.2:n.718C=
ENST00000630287.2:c.510C= ENSP00000486694.1:p.Ile170=
NM_006516.2:c.510C= NP_006507.2:p.Ile170=
NM_006516.3:c.510C= NP_006507.2:p.Ile170=
NM_006516.4:c.510C= MANE Select NP_006507.2:p.Ile170=