Canonical Allele Identifier: CA1165412390
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929753T= , CM000663.2:g.42929753T= GRCh38
NC_000001.10:g.43395424T= , CM000663.1:g.43395424T= GRCh37
NC_000001.9:g.43168011T= NCBI36
NG_008232.1:g.34424A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.707A= MANE Select ENSP00000416293.2:p.Asp236=
ENST00000669445.1:c.57-20A=
ENST00000674765.1:c.707A= ENSP00000501811.1:p.Asp236=
ENST00000675112.1:n.730A=
ENST00000676254.1:n.1156A=
ENST00000426263.7:c.707A= ENSP00000416293.2:p.Asp236=
ENST00000439722.2:c.586A= ENSP00000395521.2:n.586A=
ENST00000475162.3:c.415+873A=
ENST00000630287.2:c.*22A= ENSP00000486694.1:n.*22A=
NM_006516.2:c.707A= NP_006507.2:p.Asp236=
NM_006516.3:c.707A= NP_006507.2:p.Asp236=
NM_006516.4:c.707A= MANE Select NP_006507.2:p.Asp236=