Canonical Allele Identifier: CA1141188989
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930864C= , CM000663.2:g.42930864C= GRCh38
NC_000001.10:g.43396535C= , CM000663.1:g.43396535C= GRCh37
NC_000001.9:g.43169122C= NCBI36
NG_008232.1:g.33313G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.278G= MANE Select ENSP00000416293.2:p.Arg93=
ENST00000674765.1:c.278G= ENSP00000501811.1:p.Arg93=
ENST00000675112.1:n.301G=
ENST00000676254.1:n.727G=
ENST00000372500.4:c.182G= ENSP00000361578.4:p.Arg61=
ENST00000426263.7:c.278G= ENSP00000416293.2:p.Arg93=
ENST00000439722.2:c.157G= ENSP00000395521.2:n.157G=
ENST00000475162.3:c.177G=
ENST00000625233.2:n.486G=
ENST00000630287.2:c.278G= ENSP00000486694.1:p.Arg93=
NM_006516.2:c.278G= NP_006507.2:p.Arg93=
NM_006516.3:c.278G= NP_006507.2:p.Arg93=
NM_006516.4:c.278G= MANE Select NP_006507.2:p.Arg93=