Canonical Allele Identifier: CA1165411571
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927786T= , CM000663.2:g.42927786T= GRCh38
NC_000001.10:g.43393457T= , CM000663.1:g.43393457T= GRCh37
NC_000001.9:g.43166044T= NCBI36
NG_008232.1:g.36391A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1097A= MANE Select ENSP00000416293.2:p.Tyr366=
ENST00000674545.1:n.1714A=
ENST00000674765.1:c.1030-929A= ENSP00000501811.1:n.1030-929A=
ENST00000675112.1:n.1398A=
ENST00000676254.1:n.1546A=
ENST00000426263.7:c.1097A= ENSP00000416293.2:p.Tyr366=
ENST00000475162.3:c.416-808A=
ENST00000630287.2:c.*412A= ENSP00000486694.1:n.*412A=
NM_006516.2:c.1097A= NP_006507.2:p.Tyr366=
NM_006516.3:c.1097A= NP_006507.2:p.Tyr366=
NM_006516.4:c.1097A= MANE Select NP_006507.2:p.Tyr366=