Canonical Allele Identifier: CA1165412737
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930641G= , CM000663.2:g.42930641G= GRCh38
NC_000001.10:g.43396312G= , CM000663.1:g.43396312G= GRCh37
NC_000001.9:g.43168899G= NCBI36
NG_008232.1:g.33536C=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.501C= MANE Select ENSP00000416293.2:p.Gly167=
ENST00000674765.1:c.501C= ENSP00000501811.1:p.Gly167=
ENST00000675112.1:n.524C=
ENST00000676254.1:n.950C=
ENST00000426263.7:c.501C= ENSP00000416293.2:p.Gly167=
ENST00000439722.2:c.380C= ENSP00000395521.2:n.380C=
ENST00000475162.3:c.400C=
ENST00000625233.2:n.709C=
ENST00000630287.2:c.501C= ENSP00000486694.1:p.Gly167=
NM_006516.2:c.501C= NP_006507.2:p.Gly167=
NM_006516.3:c.501C= NP_006507.2:p.Gly167=
NM_006516.4:c.501C= MANE Select NP_006507.2:p.Gly167=