Canonical Allele Identifier: CA1165411569
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927780C= , CM000663.2:g.42927780C= GRCh38
NC_000001.10:g.43393451C= , CM000663.1:g.43393451C= GRCh37
NC_000001.9:g.43166038C= NCBI36
NG_008232.1:g.36397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1103G= MANE Select ENSP00000416293.2:p.Ser368=
ENST00000674545.1:n.1720G=
ENST00000674765.1:c.1030-923G= ENSP00000501811.1:n.1030-923G=
ENST00000675112.1:n.1404G=
ENST00000676254.1:n.1552G=
ENST00000426263.7:c.1103G= ENSP00000416293.2:p.Ser368=
ENST00000475162.3:c.416-802G=
ENST00000630287.2:c.*418G= ENSP00000486694.1:n.*418G=
NM_006516.2:c.1103G= NP_006507.2:p.Ser368=
NM_006516.3:c.1103G= NP_006507.2:p.Ser368=
NM_006516.4:c.1103G= MANE Select NP_006507.2:p.Ser368=