Canonical Allele Identifier: CA1141472781
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930635G= , CM000663.2:g.42930635G= GRCh38
NC_000001.10:g.43396306G= , CM000663.1:g.43396306G= GRCh37
NC_000001.9:g.43168893G= NCBI36
NG_008232.1:g.33542C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.507C= MANE Select ENSP00000416293.2:p.Leu169=
ENST00000674765.1:c.507C= ENSP00000501811.1:p.Leu169=
ENST00000675112.1:n.530C=
ENST00000676254.1:n.956C=
ENST00000426263.7:c.507C= ENSP00000416293.2:p.Leu169=
ENST00000439722.2:c.386C= ENSP00000395521.2:n.386C=
ENST00000475162.3:c.406C=
ENST00000625233.2:n.715C=
ENST00000630287.2:c.507C= ENSP00000486694.1:p.Leu169=
NM_006516.2:c.507C= NP_006507.2:p.Leu169=
NM_006516.3:c.507C= NP_006507.2:p.Leu169=
NM_006516.4:c.507C= MANE Select NP_006507.2:p.Leu169=