Canonical Allele Identifier: CA1165412187
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929258A= , CM000663.2:g.42929258A= GRCh38
NC_000001.10:g.43394929A= , CM000663.1:g.43394929A= GRCh37
NC_000001.9:g.43167516A= NCBI36
NG_008232.1:g.34919T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.924T= MANE Select ENSP00000416293.2:p.Tyr308=
ENST00000674545.1:n.242T=
ENST00000674765.1:c.924T= ENSP00000501811.1:p.Tyr308=
ENST00000675112.1:n.1225T=
ENST00000676254.1:n.1373T=
ENST00000426263.7:c.924T= ENSP00000416293.2:p.Tyr308=
ENST00000439722.2:c.803T= ENSP00000395521.2:n.803T=
ENST00000475162.3:c.415+1368T=
ENST00000630287.2:c.*239T= ENSP00000486694.1:n.*239T=
NM_006516.2:c.924T= NP_006507.2:p.Tyr308=
NM_006516.3:c.924T= NP_006507.2:p.Tyr308=
NM_006516.4:c.924T= MANE Select NP_006507.2:p.Tyr308=