Canonical Allele Identifier: CA1165411319
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927149G= , CM000663.2:g.42927149G= GRCh38
NC_000001.10:g.43392820G= , CM000663.1:g.43392820G= GRCh37
NC_000001.9:g.43165407G= NCBI36
NG_008232.1:g.37028C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1371C= MANE Select ENSP00000416293.2:p.Gly457=
ENST00000674545.1:n.1988C=
ENST00000674765.1:c.1030-292C= ENSP00000501811.1:n.1030-292C=
ENST00000675112.1:n.1672C=
ENST00000676254.1:n.1820C=
ENST00000426263.7:c.1371C= ENSP00000416293.2:p.Gly457=
ENST00000475162.3:c.416-171C=
ENST00000630287.2:c.*686C= ENSP00000486694.1:n.*686C=
NM_006516.2:c.1371C= NP_006507.2:p.Gly457=
NM_006516.3:c.1371C= NP_006507.2:p.Gly457=
NM_006516.4:c.1371C= MANE Select NP_006507.2:p.Gly457=