Canonical Allele Identifier: CA1165412734
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930631C= , CM000663.2:g.42930631C= GRCh38
NC_000001.10:g.43396302C= , CM000663.1:g.43396302C= GRCh37
NC_000001.9:g.43168889C= NCBI36
NG_008232.1:g.33546G=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.511G= MANE Select ENSP00000416293.2:p.Ala171=
ENST00000674765.1:c.511G= ENSP00000501811.1:p.Ala171=
ENST00000675112.1:n.534G=
ENST00000676254.1:n.960G=
ENST00000426263.7:c.511G= ENSP00000416293.2:p.Ala171=
ENST00000439722.2:c.390G= ENSP00000395521.2:n.390G=
ENST00000475162.3:c.410G=
ENST00000625233.2:n.719G=
ENST00000630287.2:c.511G= ENSP00000486694.1:p.Ala171=
NM_006516.2:c.511G= NP_006507.2:p.Ala171=
NM_006516.3:c.511G= NP_006507.2:p.Ala171=
NM_006516.4:c.511G= MANE Select NP_006507.2:p.Ala171=