Canonical Allele Identifier: CA339960150
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930628G>C , CM000663.2:g.42930628G>C GRCh38
NC_000001.10:g.43396299G>C , CM000663.1:g.43396299G>C GRCh37
NC_000001.9:g.43168886G>C NCBI36
NG_008232.1:g.33549C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.514C>G MANE Select ENSP00000416293.2:p.Gln172Glu
ENST00000674765.1:c.514C>G ENSP00000501811.1:p.Gln172Glu
ENST00000675112.1:n.537C>G
ENST00000676254.1:n.963C>G
ENST00000426263.7:c.514C>G ENSP00000416293.2:p.Gln172Glu
ENST00000439722.2:c.393C>G ENSP00000395521.2:n.393C>G
ENST00000475162.3:c.413C>G
ENST00000625233.2:n.722C>G
ENST00000630287.2:c.514C>G ENSP00000486694.1:p.Gln172Glu
NM_006516.2:c.514C>G NP_006507.2:p.Gln172Glu
NM_006516.3:c.514C>G NP_006507.2:p.Gln172Glu
NM_006516.4:c.514C>G MANE Select NP_006507.2:p.Gln172Glu