Canonical Allele Identifier: CA1165412759
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930685G= , CM000663.2:g.42930685G= GRCh38
NC_000001.10:g.43396356G= , CM000663.1:g.43396356G= GRCh37
NC_000001.9:g.43168943G= NCBI36
NG_008232.1:g.33492C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.457C= MANE Select ENSP00000416293.2:p.Arg153=
ENST00000674765.1:c.457C= ENSP00000501811.1:p.Arg153=
ENST00000675112.1:n.480C=
ENST00000676254.1:n.906C=
ENST00000426263.7:c.457C= ENSP00000416293.2:p.Arg153=
ENST00000439722.2:c.336C= ENSP00000395521.2:n.336C=
ENST00000475162.3:c.356C=
ENST00000625233.2:n.665C=
ENST00000630287.2:c.457C= ENSP00000486694.1:p.Arg153=
NM_006516.2:c.457C= NP_006507.2:p.Arg153=
NM_006516.3:c.457C= NP_006507.2:p.Arg153=
NM_006516.4:c.457C= MANE Select NP_006507.2:p.Arg153=