Canonical Allele Identifier: CA1142361047
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929596G= , CM000663.2:g.42929596G= GRCh38
NC_000001.10:g.43395267G= , CM000663.1:g.43395267G= GRCh37
NC_000001.9:g.43167854G= NCBI36
NG_008232.1:g.34581C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.864C= MANE Select ENSP00000416293.2:p.Asn288=
ENST00000674765.1:c.864C= ENSP00000501811.1:p.Asn288=
ENST00000675112.1:n.887C=
ENST00000676254.1:n.1313C=
ENST00000426263.7:c.864C= ENSP00000416293.2:p.Asn288=
ENST00000439722.2:c.743C= ENSP00000395521.2:n.743C=
ENST00000475162.3:c.415+1030C=
ENST00000630287.2:c.*179C= ENSP00000486694.1:n.*179C=
NM_006516.2:c.864C= NP_006507.2:p.Asn288=
NM_006516.3:c.864C= NP_006507.2:p.Asn288=
NM_006516.4:c.864C= MANE Select NP_006507.2:p.Asn288=