Canonical Allele Identifier: CA1139927433
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42949617G= , CM000663.2:g.42949617G= GRCh38
NC_000001.10:g.43415288G= , CM000663.1:g.43415288G= GRCh37
NC_000001.9:g.43187875G= NCBI36
NG_008232.1:g.14560C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-6296C= MANE Select ENSP00000416293.2:n.19-6296C=
ENST00000674765.1:c.19-6296C= ENSP00000501811.1:n.19-6296C=
ENST00000675112.1:n.42-6296C=
ENST00000372500.4:c.18+9017C= ENSP00000361578.4:n.18+9017C=
ENST00000415851.6:n.236-6296C=
ENST00000426263.7:c.19-6296C= ENSP00000416293.2:n.19-6296C=
ENST00000625233.2:n.227-6296C=
ENST00000628173.1:n.238-6296C=
ENST00000630287.2:c.19-6296C= ENSP00000486694.1:n.19-6296C=
ENST00000630821.1:n.236-6296C=
NM_006516.2:c.19-6296C= NP_006507.2:n.19-6296C=
NM_006516.3:c.19-6296C= NP_006507.2:n.19-6296C=
NM_006516.4:c.19-6296C= MANE Select NP_006507.2:n.19-6296C=