Canonical Allele Identifier: CA339956569
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929247C>G , CM000663.2:g.42929247C>G GRCh38
NC_000001.10:g.43394918C>G , CM000663.1:g.43394918C>G GRCh37
NC_000001.9:g.43167505C>G NCBI36
NG_008232.1:g.34930G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.935G>C MANE Select ENSP00000416293.2:p.Gly312Ala
ENST00000674545.1:n.253G>C
ENST00000674765.1:c.935G>C ENSP00000501811.1:p.Gly312Ala
ENST00000675112.1:n.1236G>C
ENST00000676254.1:n.1384G>C
ENST00000426263.7:c.935G>C ENSP00000416293.2:p.Gly312Ala
ENST00000439722.2:c.814G>C ENSP00000395521.2:n.814G>C
ENST00000475162.3:c.415+1379G>C
ENST00000630287.2:c.*250G>C ENSP00000486694.1:n.*250G>C
NM_006516.2:c.935G>C NP_006507.2:p.Gly312Ala
NM_006516.3:c.935G>C NP_006507.2:p.Gly312Ala
NM_006516.4:c.935G>C MANE Select NP_006507.2:p.Gly312Ala