Canonical Allele Identifier: CA1165417698
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943043T= , CM000663.2:g.42943043T= GRCh38
NC_000001.10:g.43408714T= , CM000663.1:g.43408714T= GRCh37
NC_000001.9:g.43181301T= NCBI36
NG_008232.1:g.21134A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.114+183A= MANE Select ENSP00000416293.2:n.114+183A=
ENST00000674765.1:c.114+183A= ENSP00000501811.1:n.114+183A=
ENST00000675112.1:n.137+183A=
ENST00000372500.4:c.19-11837A= ENSP00000361578.4:n.19-11837A=
ENST00000415851.6:n.331+183A=
ENST00000426263.7:c.114+183A= ENSP00000416293.2:n.114+183A=
ENST00000475162.3:c.13+183A=
ENST00000625233.2:n.322+183A=
ENST00000628173.1:n.333+183A=
ENST00000630287.2:c.114+183A= ENSP00000486694.1:n.114+183A=
ENST00000630821.1:n.514A=
NM_006516.2:c.114+183A= NP_006507.2:n.114+183A=
NM_006516.3:c.114+183A= NP_006507.2:n.114+183A=
NM_006516.4:c.114+183A= MANE Select NP_006507.2:n.114+183A=