Canonical Allele Identifier: CA1165412765
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930699G= , CM000663.2:g.42930699G= GRCh38
NC_000001.10:g.43396370G= , CM000663.1:g.43396370G= GRCh37
NC_000001.9:g.43168957G= NCBI36
NG_008232.1:g.33478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.443C= MANE Select ENSP00000416293.2:p.Ser148=
ENST00000674765.1:c.443C= ENSP00000501811.1:p.Ser148=
ENST00000675112.1:n.466C=
ENST00000676254.1:n.892C=
ENST00000372500.4:c.347C= ENSP00000361578.4:p.Ser116=
ENST00000426263.7:c.443C= ENSP00000416293.2:p.Ser148=
ENST00000439722.2:c.322C= ENSP00000395521.2:n.322C=
ENST00000475162.3:c.342C=
ENST00000625233.2:n.651C=
ENST00000630287.2:c.443C= ENSP00000486694.1:p.Ser148=
NM_006516.2:c.443C= NP_006507.2:p.Ser148=
NM_006516.3:c.443C= NP_006507.2:p.Ser148=
NM_006516.4:c.443C= MANE Select NP_006507.2:p.Ser148=