Canonical Allele Identifier: CA339960812
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930732G>A , CM000663.2:g.42930732G>A GRCh38
NC_000001.10:g.43396403G>A , CM000663.1:g.43396403G>A GRCh37
NC_000001.9:g.43168990G>A NCBI36
NG_008232.1:g.33445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.410C>T MANE Select ENSP00000416293.2:p.Thr137Ile
ENST00000674765.1:c.410C>T ENSP00000501811.1:p.Thr137Ile
ENST00000675112.1:n.433C>T
ENST00000676254.1:n.859C>T
ENST00000372500.4:c.314C>T ENSP00000361578.4:p.Thr105Ile
ENST00000426263.7:c.410C>T ENSP00000416293.2:p.Thr137Ile
ENST00000439722.2:c.289C>T ENSP00000395521.2:n.289C>T
ENST00000475162.3:c.309C>T
ENST00000625233.2:n.618C>T
ENST00000630287.2:c.410C>T ENSP00000486694.1:p.Thr137Ile
NM_006516.2:c.410C>T NP_006507.2:p.Thr137Ile
NM_006516.3:c.410C>T NP_006507.2:p.Thr137Ile
NM_006516.4:c.410C>T MANE Select NP_006507.2:p.Thr137Ile