Canonical Allele Identifier: CA339956137
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929027C>G , CM000663.2:g.42929027C>G GRCh38
NC_000001.10:g.43394698C>G , CM000663.1:g.43394698C>G GRCh37
NC_000001.9:g.43167285C>G NCBI36
NG_008232.1:g.35150G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.979G>C MANE Select ENSP00000416293.2:p.Val327Leu
ENST00000674545.1:n.473G>C
ENST00000674765.1:c.979G>C ENSP00000501811.1:p.Val327Leu
ENST00000675112.1:n.1280G>C
ENST00000676254.1:n.1428G>C
ENST00000426263.7:c.979G>C ENSP00000416293.2:p.Val327Leu
ENST00000439722.2:c.858G>C ENSP00000395521.2:n.858G>C
ENST00000475162.3:c.415+1599G>C
ENST00000630287.2:c.*294G>C ENSP00000486694.1:n.*294G>C
NM_006516.2:c.979G>C NP_006507.2:p.Val327Leu
NM_006516.3:c.979G>C NP_006507.2:p.Val327Leu
NM_006516.4:c.979G>C MANE Select NP_006507.2:p.Val327Leu