Canonical Allele Identifier: CA1147812489
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929663G= , CM000663.2:g.42929663G= GRCh38
NC_000001.10:g.43395334G= , CM000663.1:g.43395334G= GRCh37
NC_000001.9:g.43167921G= NCBI36
NG_008232.1:g.34514C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.797C= MANE Select ENSP00000416293.2:p.Pro266=
ENST00000669445.1:c.127C=
ENST00000674765.1:c.797C= ENSP00000501811.1:p.Pro266=
ENST00000675112.1:n.820C=
ENST00000676254.1:n.1246C=
ENST00000426263.7:c.797C= ENSP00000416293.2:p.Pro266=
ENST00000439722.2:c.676C= ENSP00000395521.2:n.676C=
ENST00000475162.3:c.415+963C=
ENST00000630287.2:c.*112C= ENSP00000486694.1:n.*112C=
NM_006516.2:c.797C= NP_006507.2:p.Pro266=
NM_006516.3:c.797C= NP_006507.2:p.Pro266=
NM_006516.4:c.797C= MANE Select NP_006507.2:p.Pro266=