Canonical Allele Identifier: CA1165411557
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927749G= , CM000663.2:g.42927749G= GRCh38
NC_000001.10:g.43393420G= , CM000663.1:g.43393420G= GRCh37
NC_000001.9:g.43166007G= NCBI36
NG_008232.1:g.36428C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1134C= MANE Select ENSP00000416293.2:p.Phe378=
ENST00000674545.1:n.1751C=
ENST00000674765.1:c.1030-892C= ENSP00000501811.1:n.1030-892C=
ENST00000675112.1:n.1435C=
ENST00000676254.1:n.1583C=
ENST00000426263.7:c.1134C= ENSP00000416293.2:p.Phe378=
ENST00000475162.3:c.416-771C=
ENST00000630287.2:c.*449C= ENSP00000486694.1:n.*449C=
NM_006516.2:c.1134C= NP_006507.2:p.Phe378=
NM_006516.3:c.1134C= NP_006507.2:p.Phe378=
NM_006516.4:c.1134C= MANE Select NP_006507.2:p.Phe378=