Canonical Allele Identifier: CA1165411608
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927870A= , CM000663.2:g.42927870A= GRCh38
NC_000001.10:g.43393541A= , CM000663.1:g.43393541A= GRCh37
NC_000001.9:g.43166128A= NCBI36
NG_008232.1:g.36307T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1075-62T= MANE Select ENSP00000416293.2:n.1075-62T=
ENST00000674545.1:n.1630T=
ENST00000674765.1:c.1030-1013T= ENSP00000501811.1:n.1030-1013T=
ENST00000675112.1:n.1376-62T=
ENST00000676254.1:n.1524-62T=
ENST00000426263.7:c.1075-62T= ENSP00000416293.2:n.1075-62T=
ENST00000475162.3:c.416-892T=
ENST00000630287.2:c.*390-62T= ENSP00000486694.1:n.*390-62T=
NM_006516.2:c.1075-62T= NP_006507.2:n.1075-62T=
NM_006516.3:c.1075-62T= NP_006507.2:n.1075-62T=
NM_006516.4:c.1075-62T= MANE Select NP_006507.2:n.1075-62T=