Canonical Allele Identifier: CA1165412353
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929669C= , CM000663.2:g.42929669C= GRCh38
NC_000001.10:g.43395340C= , CM000663.1:g.43395340C= GRCh37
NC_000001.9:g.43167927C= NCBI36
NG_008232.1:g.34508G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.791G= MANE Select ENSP00000416293.2:p.Arg264=
ENST00000669445.1:c.121G=
ENST00000674765.1:c.791G= ENSP00000501811.1:p.Arg264=
ENST00000675112.1:n.814G=
ENST00000676254.1:n.1240G=
ENST00000426263.7:c.791G= ENSP00000416293.2:p.Arg264=
ENST00000439722.2:c.670G= ENSP00000395521.2:n.670G=
ENST00000475162.3:c.415+957G=
ENST00000630287.2:c.*106G= ENSP00000486694.1:n.*106G=
NM_006516.2:c.791G= NP_006507.2:p.Arg264=
NM_006516.3:c.791G= NP_006507.2:p.Arg264=
NM_006516.4:c.791G= MANE Select NP_006507.2:p.Arg264=