Canonical Allele Identifier: CA1165412549
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930173G= , CM000663.2:g.42930173G= GRCh38
NC_000001.10:g.43395844G= , CM000663.1:g.43395844G= GRCh37
NC_000001.9:g.43168431G= NCBI36
NG_008232.1:g.34004C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-138C= MANE Select ENSP00000416293.2:n.517-138C=
ENST00000674765.1:c.517-138C= ENSP00000501811.1:n.517-138C=
ENST00000675112.1:n.540-138C=
ENST00000676254.1:n.966-138C=
ENST00000426263.7:c.517-138C= ENSP00000416293.2:n.517-138C=
ENST00000439722.2:c.396-138C= ENSP00000395521.2:n.396-138C=
ENST00000475162.3:c.415+453C=
ENST00000630287.2:c.517-393C= ENSP00000486694.1:n.517-393C=
NM_006516.2:c.517-138C= NP_006507.2:n.517-138C=
NM_006516.3:c.517-138C= NP_006507.2:n.517-138C=
NM_006516.4:c.517-138C= MANE Select NP_006507.2:n.517-138C=