Canonical Allele Identifier: CA339956622
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929253G>T , CM000663.2:g.42929253G>T GRCh38
NC_000001.10:g.43394924G>T , CM000663.1:g.43394924G>T GRCh37
NC_000001.9:g.43167511G>T NCBI36
NG_008232.1:g.34924C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.929C>A MANE Select ENSP00000416293.2:p.Thr310Asn
ENST00000674545.1:n.247C>A
ENST00000674765.1:c.929C>A ENSP00000501811.1:p.Thr310Asn
ENST00000675112.1:n.1230C>A
ENST00000676254.1:n.1378C>A
ENST00000426263.7:c.929C>A ENSP00000416293.2:p.Thr310Asn
ENST00000439722.2:c.808C>A ENSP00000395521.2:n.808C>A
ENST00000475162.3:c.415+1373C>A
ENST00000630287.2:c.*244C>A ENSP00000486694.1:n.*244C>A
NM_006516.2:c.929C>A NP_006507.2:p.Thr310Asn
NM_006516.3:c.929C>A NP_006507.2:p.Thr310Asn
NM_006516.4:c.929C>A MANE Select NP_006507.2:p.Thr310Asn