Canonical Allele Identifier: CA339956375
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929224A>C , CM000663.2:g.42929224A>C GRCh38
NC_000001.10:g.43394895A>C , CM000663.1:g.43394895A>C GRCh37
NC_000001.9:g.43167482A>C NCBI36
NG_008232.1:g.34953T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.958T>G MANE Select ENSP00000416293.2:p.Phe320Val
ENST00000674545.1:n.276T>G
ENST00000674765.1:c.958T>G ENSP00000501811.1:p.Phe320Val
ENST00000675112.1:n.1259T>G
ENST00000676254.1:n.1407T>G
ENST00000426263.7:c.958T>G ENSP00000416293.2:p.Phe320Val
ENST00000439722.2:c.837T>G ENSP00000395521.2:n.837T>G
ENST00000475162.3:c.415+1402T>G
ENST00000630287.2:c.*273T>G ENSP00000486694.1:n.*273T>G
NM_006516.2:c.958T>G NP_006507.2:p.Phe320Val
NM_006516.3:c.958T>G NP_006507.2:p.Phe320Val
NM_006516.4:c.958T>G MANE Select NP_006507.2:p.Phe320Val