Canonical Allele Identifier: CA1165412790
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930778G= , CM000663.2:g.42930778G= GRCh38
NC_000001.10:g.43396449G= , CM000663.1:g.43396449G= GRCh37
NC_000001.9:g.43169036G= NCBI36
NG_008232.1:g.33399C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.364C= MANE Select ENSP00000416293.2:p.Leu122=
ENST00000674765.1:c.364C= ENSP00000501811.1:p.Leu122=
ENST00000675112.1:n.387C=
ENST00000676254.1:n.813C=
ENST00000372500.4:c.268C= ENSP00000361578.4:p.Leu90=
ENST00000426263.7:c.364C= ENSP00000416293.2:p.Leu122=
ENST00000439722.2:c.243C= ENSP00000395521.2:n.243C=
ENST00000475162.3:c.263C=
ENST00000625233.2:n.572C=
ENST00000630287.2:c.364C= ENSP00000486694.1:p.Leu122=
NM_006516.2:c.364C= NP_006507.2:p.Leu122=
NM_006516.3:c.364C= NP_006507.2:p.Leu122=
NM_006516.4:c.364C= MANE Select NP_006507.2:p.Leu122=