Canonical Allele Identifier: CA339956461
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929235A>T , CM000663.2:g.42929235A>T GRCh38
NC_000001.10:g.43394906A>T , CM000663.1:g.43394906A>T GRCh37
NC_000001.9:g.43167493A>T NCBI36
NG_008232.1:g.34942T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.947T>A MANE Select ENSP00000416293.2:p.Val316Asp
ENST00000674545.1:n.265T>A
ENST00000674765.1:c.947T>A ENSP00000501811.1:p.Val316Asp
ENST00000675112.1:n.1248T>A
ENST00000676254.1:n.1396T>A
ENST00000426263.7:c.947T>A ENSP00000416293.2:p.Val316Asp
ENST00000439722.2:c.826T>A ENSP00000395521.2:n.826T>A
ENST00000475162.3:c.415+1391T>A
ENST00000630287.2:c.*262T>A ENSP00000486694.1:n.*262T>A
NM_006516.2:c.947T>A NP_006507.2:p.Val316Asp
NM_006516.3:c.947T>A NP_006507.2:p.Val316Asp
NM_006516.4:c.947T>A MANE Select NP_006507.2:p.Val316Asp