Canonical Allele Identifier: CA339958656
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929972A>C , CM000663.2:g.42929972A>C GRCh38
NC_000001.10:g.43395643A>C , CM000663.1:g.43395643A>C GRCh37
NC_000001.9:g.43168230A>C NCBI36
NG_008232.1:g.34205T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.580T>G MANE Select ENSP00000416293.2:p.Phe194Val
ENST00000674765.1:c.580T>G ENSP00000501811.1:p.Phe194Val
ENST00000675112.1:n.603T>G
ENST00000676254.1:n.1029T>G
ENST00000426263.7:c.580T>G ENSP00000416293.2:p.Phe194Val
ENST00000439722.2:c.459T>G ENSP00000395521.2:n.459T>G
ENST00000475162.3:c.415+654T>G
ENST00000630287.2:c.517-192T>G ENSP00000486694.1:n.517-192T>G
NM_006516.2:c.580T>G NP_006507.2:p.Phe194Val
NM_006516.3:c.580T>G NP_006507.2:p.Phe194Val
NM_006516.4:c.580T>G MANE Select NP_006507.2:p.Phe194Val