Canonical Allele Identifier: CA1165412178
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929220G= , CM000663.2:g.42929220G= GRCh38
NC_000001.10:g.43394891G= , CM000663.1:g.43394891G= GRCh37
NC_000001.9:g.43167478G= NCBI36
NG_008232.1:g.34957C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.962C= MANE Select ENSP00000416293.2:p.Thr321=
ENST00000674545.1:n.280C=
ENST00000674765.1:c.962C= ENSP00000501811.1:p.Thr321=
ENST00000675112.1:n.1263C=
ENST00000676254.1:n.1411C=
ENST00000426263.7:c.962C= ENSP00000416293.2:p.Thr321=
ENST00000439722.2:c.841C= ENSP00000395521.2:n.841C=
ENST00000475162.3:c.415+1406C=
ENST00000630287.2:c.*277C= ENSP00000486694.1:n.*277C=
NM_006516.2:c.962C= NP_006507.2:p.Thr321=
NM_006516.3:c.962C= NP_006507.2:p.Thr321=
NM_006516.4:c.962C= MANE Select NP_006507.2:p.Thr321=