Canonical Allele Identifier: CA1165412215
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1643462036

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929331dup , CM000663.2:g.42929331dup GRCh38
NC_000001.10:g.43395002dup , CM000663.1:g.43395002dup GRCh37
NC_000001.9:g.43167589dup NCBI36
NG_008232.1:g.34848dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.868-15dup MANE Select ENSP00000416293.2:n.868-15dup
ENST00000674545.1:n.171dup
ENST00000674765.1:c.868-15dup ENSP00000501811.1:n.868-15dup
ENST00000675112.1:n.1154dup
ENST00000676254.1:n.1317-15dup
ENST00000426263.7:c.868-15dup ENSP00000416293.2:n.868-15dup
ENST00000439722.2:c.747-15dup ENSP00000395521.2:n.747-15dup
ENST00000475162.3:c.415+1297dup
ENST00000630287.2:c.*183-15dup ENSP00000486694.1:n.*183-15dup
NM_006516.2:c.868-15dup NP_006507.2:n.868-15dup
NM_006516.3:c.868-15dup NP_006507.2:n.868-15dup
NM_006516.4:c.868-15dup MANE Select NP_006507.2:n.868-15dup