Canonical Allele Identifier: CA339960554
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930685G>C , CM000663.2:g.42930685G>C GRCh38
NC_000001.10:g.43396356G>C , CM000663.1:g.43396356G>C GRCh37
NC_000001.9:g.43168943G>C NCBI36
NG_008232.1:g.33492C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.457C>G MANE Select ENSP00000416293.2:p.Arg153Gly
ENST00000674765.1:c.457C>G ENSP00000501811.1:p.Arg153Gly
ENST00000675112.1:n.480C>G
ENST00000676254.1:n.906C>G
ENST00000426263.7:c.457C>G ENSP00000416293.2:p.Arg153Gly
ENST00000439722.2:c.336C>G ENSP00000395521.2:n.336C>G
ENST00000475162.3:c.356C>G
ENST00000625233.2:n.665C>G
ENST00000630287.2:c.457C>G ENSP00000486694.1:p.Arg153Gly
NM_006516.2:c.457C>G NP_006507.2:p.Arg153Gly
NM_006516.3:c.457C>G NP_006507.2:p.Arg153Gly
NM_006516.4:c.457C>G MANE Select NP_006507.2:p.Arg153Gly