Canonical Allele Identifier: CA339960855
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930741C>T , CM000663.2:g.42930741C>T GRCh38
NC_000001.10:g.43396412C>T , CM000663.1:g.43396412C>T GRCh37
NC_000001.9:g.43168999C>T NCBI36
NG_008232.1:g.33436G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.401G>A MANE Select ENSP00000416293.2:p.Gly134Asp
ENST00000674765.1:c.401G>A ENSP00000501811.1:p.Gly134Asp
ENST00000675112.1:n.424G>A
ENST00000676254.1:n.850G>A
ENST00000372500.4:c.305G>A ENSP00000361578.4:p.Gly102Asp
ENST00000426263.7:c.401G>A ENSP00000416293.2:p.Gly134Asp
ENST00000439722.2:c.280G>A ENSP00000395521.2:n.280G>A
ENST00000475162.3:c.300G>A
ENST00000625233.2:n.609G>A
ENST00000630287.2:c.401G>A ENSP00000486694.1:p.Gly134Asp
NM_006516.2:c.401G>A NP_006507.2:p.Gly134Asp
NM_006516.3:c.401G>A NP_006507.2:p.Gly134Asp
NM_006516.4:c.401G>A MANE Select NP_006507.2:p.Gly134Asp