Canonical Allele Identifier: CA339954490
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927806C>G , CM000663.2:g.42927806C>G GRCh38
NC_000001.10:g.43393477C>G , CM000663.1:g.43393477C>G GRCh37
NC_000001.9:g.43166064C>G NCBI36
NG_008232.1:g.36371G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1077G>C MANE Select ENSP00000416293.2:p.Glu359Asp
ENST00000674545.1:n.1694G>C
ENST00000674765.1:c.1030-949G>C ENSP00000501811.1:n.1030-949G>C
ENST00000675112.1:n.1378G>C
ENST00000676254.1:n.1526G>C
ENST00000426263.7:c.1077G>C ENSP00000416293.2:p.Glu359Asp
ENST00000475162.3:c.416-828G>C
ENST00000630287.2:c.*392G>C ENSP00000486694.1:n.*392G>C
NM_006516.2:c.1077G>C NP_006507.2:p.Glu359Asp
NM_006516.3:c.1077G>C NP_006507.2:p.Glu359Asp
NM_006516.4:c.1077G>C MANE Select NP_006507.2:p.Glu359Asp