Canonical Allele Identifier: CA1165412732
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930627T= , CM000663.2:g.42930627T= GRCh38
NC_000001.10:g.43396298T= , CM000663.1:g.43396298T= GRCh37
NC_000001.9:g.43168885T= NCBI36
NG_008232.1:g.33550A=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.515A= MANE Select ENSP00000416293.2:p.Gln172=
ENST00000674765.1:c.515A= ENSP00000501811.1:p.Gln172=
ENST00000675112.1:n.538A=
ENST00000676254.1:n.964A=
ENST00000426263.7:c.515A= ENSP00000416293.2:p.Gln172=
ENST00000439722.2:c.394A= ENSP00000395521.2:n.394A=
ENST00000475162.3:c.414A=
ENST00000625233.2:n.723A=
ENST00000630287.2:c.515A= ENSP00000486694.1:p.Gln172=
NM_006516.2:c.515A= NP_006507.2:p.Gln172=
NM_006516.3:c.515A= NP_006507.2:p.Gln172=
NM_006516.4:c.515A= MANE Select NP_006507.2:p.Gln172=