Canonical Allele Identifier: CA1165412172
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929212A= , CM000663.2:g.42929212A= GRCh38
NC_000001.10:g.43394883A= , CM000663.1:g.43394883A= GRCh37
NC_000001.9:g.43167470A= NCBI36
NG_008232.1:g.34965T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.970T= MANE Select ENSP00000416293.2:p.Ser324=
ENST00000674545.1:n.288T=
ENST00000674765.1:c.970T= ENSP00000501811.1:p.Ser324=
ENST00000675112.1:n.1271T=
ENST00000676254.1:n.1419T=
ENST00000426263.7:c.970T= ENSP00000416293.2:p.Ser324=
ENST00000439722.2:c.849T= ENSP00000395521.2:n.849T=
ENST00000475162.3:c.415+1414T=
ENST00000630287.2:c.*285T= ENSP00000486694.1:n.*285T=
NM_006516.2:c.970T= NP_006507.2:p.Ser324=
NM_006516.3:c.970T= NP_006507.2:p.Ser324=
NM_006516.4:c.970T= MANE Select NP_006507.2:p.Ser324=