Canonical Allele Identifier: CA1165412355
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929670G= , CM000663.2:g.42929670G= GRCh38
NC_000001.10:g.43395341G= , CM000663.1:g.43395341G= GRCh37
NC_000001.9:g.43167928G= NCBI36
NG_008232.1:g.34507C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.790C= MANE Select ENSP00000416293.2:p.Arg264=
ENST00000669445.1:c.120C=
ENST00000674765.1:c.790C= ENSP00000501811.1:p.Arg264=
ENST00000675112.1:n.813C=
ENST00000676254.1:n.1239C=
ENST00000426263.7:c.790C= ENSP00000416293.2:p.Arg264=
ENST00000439722.2:c.669C= ENSP00000395521.2:n.669C=
ENST00000475162.3:c.415+956C=
ENST00000630287.2:c.*105C= ENSP00000486694.1:n.*105C=
NM_006516.2:c.790C= NP_006507.2:p.Arg264=
NM_006516.3:c.790C= NP_006507.2:p.Arg264=
NM_006516.4:c.790C= MANE Select NP_006507.2:p.Arg264=