Canonical Allele Identifier: CA339964840
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943281A>C , CM000663.2:g.42943281A>C GRCh38
NC_000001.10:g.43408952A>C , CM000663.1:g.43408952A>C GRCh37
NC_000001.9:g.43181539A>C NCBI36
NG_008232.1:g.20896T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.59T>G MANE Select ENSP00000416293.2:p.Val20Gly
ENST00000674765.1:c.59T>G ENSP00000501811.1:p.Val20Gly
ENST00000675112.1:n.82T>G
ENST00000372500.4:c.19-12075T>G ENSP00000361578.4:n.19-12075T>G
ENST00000415851.6:n.276T>G
ENST00000426263.7:c.59T>G ENSP00000416293.2:p.Val20Gly
ENST00000625233.2:n.267T>G
ENST00000628173.1:n.278T>G
ENST00000630287.2:c.59T>G ENSP00000486694.1:p.Val20Gly
ENST00000630821.1:n.276T>G
NM_006516.2:c.59T>G NP_006507.2:p.Val20Gly
NM_006516.3:c.59T>G NP_006507.2:p.Val20Gly
NM_006516.4:c.59T>G MANE Select NP_006507.2:p.Val20Gly