Canonical Allele Identifier: CA1165412366
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929693T= , CM000663.2:g.42929693T= GRCh38
NC_000001.10:g.43395364T= , CM000663.1:g.43395364T= GRCh37
NC_000001.9:g.43167951T= NCBI36
NG_008232.1:g.34484A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.767A= MANE Select ENSP00000416293.2:p.Lys256=
ENST00000669445.1:c.97A=
ENST00000674765.1:c.767A= ENSP00000501811.1:p.Lys256=
ENST00000675112.1:n.790A=
ENST00000676254.1:n.1216A=
ENST00000426263.7:c.767A= ENSP00000416293.2:p.Lys256=
ENST00000439722.2:c.646A= ENSP00000395521.2:n.646A=
ENST00000475162.3:c.415+933A=
ENST00000630287.2:c.*82A= ENSP00000486694.1:n.*82A=
NM_006516.2:c.767A= NP_006507.2:p.Lys256=
NM_006516.3:c.767A= NP_006507.2:p.Lys256=
NM_006516.4:c.767A= MANE Select NP_006507.2:p.Lys256=