Canonical Allele Identifier: CA1141188956
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929298G= , CM000663.2:g.42929298G= GRCh38
NC_000001.10:g.43394969G= , CM000663.1:g.43394969G= GRCh37
NC_000001.9:g.43167556G= NCBI36
NG_008232.1:g.34879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.884C= MANE Select ENSP00000416293.2:p.Thr295=
ENST00000674545.1:n.202C=
ENST00000674765.1:c.884C= ENSP00000501811.1:p.Thr295=
ENST00000675112.1:n.1185C=
ENST00000676254.1:n.1333C=
ENST00000426263.7:c.884C= ENSP00000416293.2:p.Thr295=
ENST00000439722.2:c.763C= ENSP00000395521.2:n.763C=
ENST00000475162.3:c.415+1328C=
ENST00000630287.2:c.*199C= ENSP00000486694.1:n.*199C=
NM_006516.2:c.884C= NP_006507.2:p.Thr295=
NM_006516.3:c.884C= NP_006507.2:p.Thr295=
NM_006516.4:c.884C= MANE Select NP_006507.2:p.Thr295=