Canonical Allele Identifier: CA1165412569
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930214G= , CM000663.2:g.42930214G= GRCh38
NC_000001.10:g.43395885G= , CM000663.1:g.43395885G= GRCh37
NC_000001.9:g.43168472G= NCBI36
NG_008232.1:g.33963C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-179C= MANE Select ENSP00000416293.2:n.517-179C=
ENST00000674765.1:c.517-179C= ENSP00000501811.1:n.517-179C=
ENST00000675112.1:n.540-179C=
ENST00000676254.1:n.966-179C=
ENST00000426263.7:c.517-179C= ENSP00000416293.2:n.517-179C=
ENST00000439722.2:c.396-179C= ENSP00000395521.2:n.396-179C=
ENST00000475162.3:c.415+412C=
ENST00000630287.2:c.516+412C= ENSP00000486694.1:n.516+412C=
NM_006516.2:c.517-179C= NP_006507.2:n.517-179C=
NM_006516.3:c.517-179C= NP_006507.2:n.517-179C=
NM_006516.4:c.517-179C= MANE Select NP_006507.2:n.517-179C=