Canonical Allele Identifier: CA1165412783
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930752A= , CM000663.2:g.42930752A= GRCh38
NC_000001.10:g.43396423A= , CM000663.1:g.43396423A= GRCh37
NC_000001.9:g.43169010A= NCBI36
NG_008232.1:g.33425T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.390T= MANE Select ENSP00000416293.2:p.Gly130=
ENST00000674765.1:c.390T= ENSP00000501811.1:p.Gly130=
ENST00000675112.1:n.413T=
ENST00000676254.1:n.839T=
ENST00000372500.4:c.294T= ENSP00000361578.4:p.Gly98=
ENST00000426263.7:c.390T= ENSP00000416293.2:p.Gly130=
ENST00000439722.2:c.269T= ENSP00000395521.2:n.269T=
ENST00000475162.3:c.289T=
ENST00000625233.2:n.598T=
ENST00000630287.2:c.390T= ENSP00000486694.1:p.Gly130=
NM_006516.2:c.390T= NP_006507.2:p.Gly130=
NM_006516.3:c.390T= NP_006507.2:p.Gly130=
NM_006516.4:c.390T= MANE Select NP_006507.2:p.Gly130=