Canonical Allele Identifier: CA1165411602
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927863A= , CM000663.2:g.42927863A= GRCh38
NC_000001.10:g.43393534A= , CM000663.1:g.43393534A= GRCh37
NC_000001.9:g.43166121A= NCBI36
NG_008232.1:g.36314T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1075-55T= MANE Select ENSP00000416293.2:n.1075-55T=
ENST00000674545.1:n.1637T=
ENST00000674765.1:c.1030-1006T= ENSP00000501811.1:n.1030-1006T=
ENST00000675112.1:n.1376-55T=
ENST00000676254.1:n.1524-55T=
ENST00000426263.7:c.1075-55T= ENSP00000416293.2:n.1075-55T=
ENST00000475162.3:c.416-885T=
ENST00000630287.2:c.*390-55T= ENSP00000486694.1:n.*390-55T=
NM_006516.2:c.1075-55T= NP_006507.2:n.1075-55T=
NM_006516.3:c.1075-55T= NP_006507.2:n.1075-55T=
NM_006516.4:c.1075-55T= MANE Select NP_006507.2:n.1075-55T=