Canonical Allele Identifier: CA1165412594
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930300C= , CM000663.2:g.42930300C= GRCh38
NC_000001.10:g.43395971C= , CM000663.1:g.43395971C= GRCh37
NC_000001.9:g.43168558C= NCBI36
NG_008232.1:g.33877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-265G= MANE Select ENSP00000416293.2:n.517-265G=
ENST00000674765.1:c.517-265G= ENSP00000501811.1:n.517-265G=
ENST00000675112.1:n.540-265G=
ENST00000676254.1:n.966-265G=
ENST00000426263.7:c.517-265G= ENSP00000416293.2:n.517-265G=
ENST00000439722.2:c.396-265G= ENSP00000395521.2:n.396-265G=
ENST00000475162.3:c.415+326G=
ENST00000630287.2:c.516+326G= ENSP00000486694.1:n.516+326G=
NM_006516.2:c.517-265G= NP_006507.2:n.517-265G=
NM_006516.3:c.517-265G= NP_006507.2:n.517-265G=
NM_006516.4:c.517-265G= MANE Select NP_006507.2:n.517-265G=