Canonical Allele Identifier: CA1143523582
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42931047G= , CM000663.2:g.42931047G= GRCh38
NC_000001.10:g.43396718G= , CM000663.1:g.43396718G= GRCh37
NC_000001.9:g.43169305G= NCBI36
NG_008232.1:g.33130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.274C= MANE Select ENSP00000416293.2:p.Arg92=
ENST00000674765.1:c.274C= ENSP00000501811.1:p.Arg92=
ENST00000675112.1:n.297C=
ENST00000676254.1:n.723C=
ENST00000372500.4:c.178C= ENSP00000361578.4:p.Arg60=
ENST00000415851.6:n.491C=
ENST00000426263.7:c.274C= ENSP00000416293.2:p.Arg92=
ENST00000439722.2:c.79C= ENSP00000395521.2:p.Arg27=
ENST00000475162.3:c.173C=
ENST00000625233.2:n.482C=
ENST00000630287.2:c.274C= ENSP00000486694.1:p.Arg92=
NM_006516.2:c.274C= NP_006507.2:p.Arg92=
NM_006516.3:c.274C= NP_006507.2:p.Arg92=
NM_006516.4:c.274C= MANE Select NP_006507.2:p.Arg92=