Canonical Allele Identifier: CA1165412196
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929278C= , CM000663.2:g.42929278C= GRCh38
NC_000001.10:g.43394949C= , CM000663.1:g.43394949C= GRCh37
NC_000001.9:g.43167536C= NCBI36
NG_008232.1:g.34899G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.904G= MANE Select ENSP00000416293.2:p.Gly302=
ENST00000674545.1:n.222G=
ENST00000674765.1:c.904G= ENSP00000501811.1:p.Gly302=
ENST00000675112.1:n.1205G=
ENST00000676254.1:n.1353G=
ENST00000426263.7:c.904G= ENSP00000416293.2:p.Gly302=
ENST00000439722.2:c.783G= ENSP00000395521.2:n.783G=
ENST00000475162.3:c.415+1348G=
ENST00000630287.2:c.*219G= ENSP00000486694.1:n.*219G=
NM_006516.2:c.904G= NP_006507.2:p.Gly302=
NM_006516.3:c.904G= NP_006507.2:p.Gly302=
NM_006516.4:c.904G= MANE Select NP_006507.2:p.Gly302=