Canonical Allele Identifier: CA339957898
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929698C>G , CM000663.2:g.42929698C>G GRCh38
NC_000001.10:g.43395369C>G , CM000663.1:g.43395369C>G GRCh37
NC_000001.9:g.43167956C>G NCBI36
NG_008232.1:g.34479G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.762G>C MANE Select ENSP00000416293.2:p.Glu254Asp
ENST00000669445.1:c.92G>C
ENST00000674765.1:c.762G>C ENSP00000501811.1:p.Glu254Asp
ENST00000675112.1:n.785G>C
ENST00000676254.1:n.1211G>C
ENST00000426263.7:c.762G>C ENSP00000416293.2:p.Glu254Asp
ENST00000439722.2:c.641G>C ENSP00000395521.2:n.641G>C
ENST00000475162.3:c.415+928G>C
ENST00000630287.2:c.*77G>C ENSP00000486694.1:n.*77G>C
NM_006516.2:c.762G>C NP_006507.2:p.Glu254Asp
NM_006516.3:c.762G>C NP_006507.2:p.Glu254Asp
NM_006516.4:c.762G>C MANE Select NP_006507.2:p.Glu254Asp