Canonical Allele Identifier: CA1139869635
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943295G= , CM000663.2:g.42943295G= GRCh38
NC_000001.10:g.43408966G= , CM000663.1:g.43408966G= GRCh37
NC_000001.9:g.43181553G= NCBI36
NG_008232.1:g.20882C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.45C= MANE Select ENSP00000416293.2:p.Ala15=
ENST00000674765.1:c.45C= ENSP00000501811.1:p.Ala15=
ENST00000675112.1:n.68C=
ENST00000372500.4:c.19-12089C= ENSP00000361578.4:n.19-12089C=
ENST00000415851.6:n.262C=
ENST00000426263.7:c.45C= ENSP00000416293.2:p.Ala15=
ENST00000625233.2:n.253C=
ENST00000628173.1:n.264C=
ENST00000630287.2:c.45C= ENSP00000486694.1:p.Ala15=
ENST00000630821.1:n.262C=
NM_006516.2:c.45C= NP_006507.2:p.Ala15=
NM_006516.3:c.45C= NP_006507.2:p.Ala15=
NM_006516.4:c.45C= MANE Select NP_006507.2:p.Ala15=