Canonical Allele Identifier: CA339957901
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929699T>C , CM000663.2:g.42929699T>C GRCh38
NC_000001.10:g.43395370T>C , CM000663.1:g.43395370T>C GRCh37
NC_000001.9:g.43167957T>C NCBI36
NG_008232.1:g.34478A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.761A>G MANE Select ENSP00000416293.2:p.Glu254Gly
ENST00000669445.1:c.91A>G
ENST00000674765.1:c.761A>G ENSP00000501811.1:p.Glu254Gly
ENST00000675112.1:n.784A>G
ENST00000676254.1:n.1210A>G
ENST00000426263.7:c.761A>G ENSP00000416293.2:p.Glu254Gly
ENST00000439722.2:c.640A>G ENSP00000395521.2:n.640A>G
ENST00000475162.3:c.415+927A>G
ENST00000630287.2:c.*76A>G ENSP00000486694.1:n.*76A>G
NM_006516.2:c.761A>G NP_006507.2:p.Glu254Gly
NM_006516.3:c.761A>G NP_006507.2:p.Glu254Gly
NM_006516.4:c.761A>G MANE Select NP_006507.2:p.Glu254Gly