Canonical Allele Identifier: CA1165412186
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929254T= , CM000663.2:g.42929254T= GRCh38
NC_000001.10:g.43394925T= , CM000663.1:g.43394925T= GRCh37
NC_000001.9:g.43167512T= NCBI36
NG_008232.1:g.34923A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.928A= MANE Select ENSP00000416293.2:p.Thr310=
ENST00000674545.1:n.246A=
ENST00000674765.1:c.928A= ENSP00000501811.1:p.Thr310=
ENST00000675112.1:n.1229A=
ENST00000676254.1:n.1377A=
ENST00000426263.7:c.928A= ENSP00000416293.2:p.Thr310=
ENST00000439722.2:c.807A= ENSP00000395521.2:n.807A=
ENST00000475162.3:c.415+1372A=
ENST00000630287.2:c.*243A= ENSP00000486694.1:n.*243A=
NM_006516.2:c.928A= NP_006507.2:p.Thr310=
NM_006516.3:c.928A= NP_006507.2:p.Thr310=
NM_006516.4:c.928A= MANE Select NP_006507.2:p.Thr310=