Canonical Allele Identifier: CA339960936
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930757T>C , CM000663.2:g.42930757T>C GRCh38
NC_000001.10:g.43396428T>C , CM000663.1:g.43396428T>C GRCh37
NC_000001.9:g.43169015T>C NCBI36
NG_008232.1:g.33420A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.385A>G MANE Select ENSP00000416293.2:p.Ile129Val
ENST00000674765.1:c.385A>G ENSP00000501811.1:p.Ile129Val
ENST00000675112.1:n.408A>G
ENST00000676254.1:n.834A>G
ENST00000372500.4:c.289A>G ENSP00000361578.4:p.Ile97Val
ENST00000426263.7:c.385A>G ENSP00000416293.2:p.Ile129Val
ENST00000439722.2:c.264A>G ENSP00000395521.2:n.264A>G
ENST00000475162.3:c.284A>G
ENST00000625233.2:n.593A>G
ENST00000630287.2:c.385A>G ENSP00000486694.1:p.Ile129Val
NM_006516.2:c.385A>G NP_006507.2:p.Ile129Val
NM_006516.3:c.385A>G NP_006507.2:p.Ile129Val
NM_006516.4:c.385A>G MANE Select NP_006507.2:p.Ile129Val