Canonical Allele Identifier: CA1141090257
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929683G= , CM000663.2:g.42929683G= GRCh38
NC_000001.10:g.43395354G= , CM000663.1:g.43395354G= GRCh37
NC_000001.9:g.43167941G= NCBI36
NG_008232.1:g.34494C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.777C= MANE Select ENSP00000416293.2:p.Ile259=
ENST00000669445.1:c.107C=
ENST00000674765.1:c.777C= ENSP00000501811.1:p.Ile259=
ENST00000675112.1:n.800C=
ENST00000676254.1:n.1226C=
ENST00000426263.7:c.777C= ENSP00000416293.2:p.Ile259=
ENST00000439722.2:c.656C= ENSP00000395521.2:n.656C=
ENST00000475162.3:c.415+943C=
ENST00000630287.2:c.*92C= ENSP00000486694.1:n.*92C=
NM_006516.2:c.777C= NP_006507.2:p.Ile259=
NM_006516.3:c.777C= NP_006507.2:p.Ile259=
NM_006516.4:c.777C= MANE Select NP_006507.2:p.Ile259=