Canonical Allele Identifier: CA1165411504
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927597G= , CM000663.2:g.42927597G= GRCh38
NC_000001.10:g.43393268G= , CM000663.1:g.43393268G= GRCh37
NC_000001.9:g.43165855G= NCBI36
NG_008232.1:g.36580C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1278+8C= MANE Select ENSP00000416293.2:n.1278+8C=
ENST00000674545.1:n.1895+8C=
ENST00000674765.1:c.1030-740C= ENSP00000501811.1:n.1030-740C=
ENST00000675112.1:n.1579+8C=
ENST00000676254.1:n.1727+8C=
ENST00000426263.7:c.1278+8C= ENSP00000416293.2:n.1278+8C=
ENST00000475162.3:c.416-619C=
ENST00000630287.2:c.*593+8C= ENSP00000486694.1:n.*593+8C=
NM_006516.2:c.1278+8C= NP_006507.2:n.1278+8C=
NM_006516.3:c.1278+8C= NP_006507.2:n.1278+8C=
NM_006516.4:c.1278+8C= MANE Select NP_006507.2:n.1278+8C=