Canonical Allele Identifier: CA339956172
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929034C>G , CM000663.2:g.42929034C>G GRCh38
NC_000001.10:g.43394705C>G , CM000663.1:g.43394705C>G GRCh37
NC_000001.9:g.43167292C>G NCBI36
NG_008232.1:g.35143G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.973-1G>C MANE Select ENSP00000416293.2:n.973-1G>C
ENST00000674545.1:n.466G>C
ENST00000674765.1:c.973-1G>C ENSP00000501811.1:n.973-1G>C
ENST00000675112.1:n.1274-1G>C
ENST00000676254.1:n.1422-1G>C
ENST00000426263.7:c.973-1G>C ENSP00000416293.2:n.973-1G>C
ENST00000439722.2:c.852-1G>C ENSP00000395521.2:n.852-1G>C
ENST00000475162.3:c.415+1592G>C
ENST00000630287.2:c.*288-1G>C ENSP00000486694.1:n.*288-1G>C
NM_006516.2:c.973-1G>C NP_006507.2:n.973-1G>C
NM_006516.3:c.973-1G>C NP_006507.2:n.973-1G>C
NM_006516.4:c.973-1G>C MANE Select NP_006507.2:n.973-1G>C