Canonical Allele Identifier: CA1165411513
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927613A= , CM000663.2:g.42927613A= GRCh38
NC_000001.10:g.43393284A= , CM000663.1:g.43393284A= GRCh37
NC_000001.9:g.43165871A= NCBI36
NG_008232.1:g.36564T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1270T= MANE Select ENSP00000416293.2:p.Tyr424=
ENST00000674545.1:n.1887T=
ENST00000674765.1:c.1030-756T= ENSP00000501811.1:n.1030-756T=
ENST00000675112.1:n.1571T=
ENST00000676254.1:n.1719T=
ENST00000426263.7:c.1270T= ENSP00000416293.2:p.Tyr424=
ENST00000475162.3:c.416-635T=
ENST00000630287.2:c.*585T= ENSP00000486694.1:n.*585T=
NM_006516.2:c.1270T= NP_006507.2:p.Tyr424=
NM_006516.3:c.1270T= NP_006507.2:p.Tyr424=
NM_006516.4:c.1270T= MANE Select NP_006507.2:p.Tyr424=