Canonical Allele Identifier: CA1165415267
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42936959G= , CM000663.2:g.42936959G= GRCh38
NC_000001.10:g.43402630G= , CM000663.1:g.43402630G= GRCh37
NC_000001.9:g.43175217G= NCBI36
NG_008232.1:g.27218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.115-5753C= MANE Select ENSP00000416293.2:n.115-5753C=
ENST00000674765.1:c.115-5753C= ENSP00000501811.1:n.115-5753C=
ENST00000675112.1:n.138-5753C=
ENST00000372500.4:c.19-5753C= ENSP00000361578.4:n.19-5753C=
ENST00000415851.6:n.332-5753C=
ENST00000426263.7:c.115-5753C= ENSP00000416293.2:n.115-5753C=
ENST00000475162.3:c.14-5753C=
ENST00000625233.2:n.323-5753C=
ENST00000628173.1:n.460+2864C=
ENST00000630287.2:c.115-5753C= ENSP00000486694.1:n.115-5753C=
NM_006516.2:c.115-5753C= NP_006507.2:n.115-5753C=
NM_006516.3:c.115-5753C= NP_006507.2:n.115-5753C=
NM_006516.4:c.115-5753C= MANE Select NP_006507.2:n.115-5753C=