Canonical Allele Identifier: CA1165412364
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929691C= , CM000663.2:g.42929691C= GRCh38
NC_000001.10:g.43395362C= , CM000663.1:g.43395362C= GRCh37
NC_000001.9:g.43167949C= NCBI36
NG_008232.1:g.34486G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.769G= MANE Select ENSP00000416293.2:p.Val257=
ENST00000669445.1:c.99G=
ENST00000674765.1:c.769G= ENSP00000501811.1:p.Val257=
ENST00000675112.1:n.792G=
ENST00000676254.1:n.1218G=
ENST00000426263.7:c.769G= ENSP00000416293.2:p.Val257=
ENST00000439722.2:c.648G= ENSP00000395521.2:n.648G=
ENST00000475162.3:c.415+935G=
ENST00000630287.2:c.*84G= ENSP00000486694.1:n.*84G=
NM_006516.2:c.769G= NP_006507.2:p.Val257=
NM_006516.3:c.769G= NP_006507.2:p.Val257=
NM_006516.4:c.769G= MANE Select NP_006507.2:p.Val257=