Canonical Allele Identifier: CA1143404454
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929655G= , CM000663.2:g.42929655G= GRCh38
NC_000001.10:g.43395326G= , CM000663.1:g.43395326G= GRCh37
NC_000001.9:g.43167913G= NCBI36
NG_008232.1:g.34522C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.805C= MANE Select ENSP00000416293.2:p.Arg269=
ENST00000669445.1:c.135C=
ENST00000674765.1:c.805C= ENSP00000501811.1:p.Arg269=
ENST00000675112.1:n.828C=
ENST00000676254.1:n.1254C=
ENST00000426263.7:c.805C= ENSP00000416293.2:p.Arg269=
ENST00000439722.2:c.684C= ENSP00000395521.2:n.684C=
ENST00000475162.3:c.415+971C=
ENST00000630287.2:c.*120C= ENSP00000486694.1:n.*120C=
NM_006516.2:c.805C= NP_006507.2:p.Arg269=
NM_006516.3:c.805C= NP_006507.2:p.Arg269=
NM_006516.4:c.805C= MANE Select NP_006507.2:p.Arg269=