Canonical Allele Identifier: CA1165412219
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929340G= , CM000663.2:g.42929340G= GRCh38
NC_000001.10:g.43395011G= , CM000663.1:g.43395011G= GRCh37
NC_000001.9:g.43167598G= NCBI36
NG_008232.1:g.34837C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.868-26C= MANE Select ENSP00000416293.2:n.868-26C=
ENST00000674545.1:n.160C=
ENST00000674765.1:c.868-26C= ENSP00000501811.1:n.868-26C=
ENST00000675112.1:n.1143C=
ENST00000676254.1:n.1317-26C=
ENST00000426263.7:c.868-26C= ENSP00000416293.2:n.868-26C=
ENST00000439722.2:c.747-26C= ENSP00000395521.2:n.747-26C=
ENST00000475162.3:c.415+1286C=
ENST00000630287.2:c.*183-26C= ENSP00000486694.1:n.*183-26C=
NM_006516.2:c.868-26C= NP_006507.2:n.868-26C=
NM_006516.3:c.868-26C= NP_006507.2:n.868-26C=
NM_006516.4:c.868-26C= MANE Select NP_006507.2:n.868-26C=