Canonical Allele Identifier: CA339956774
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs944584284
gnomAD v2: 1-43394948-C-G
gnomAD v4: 1-42929277-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929277C>G , CM000663.2:g.42929277C>G GRCh38
NC_000001.10:g.43394948C>G , CM000663.1:g.43394948C>G GRCh37
NC_000001.9:g.43167535C>G NCBI36
NG_008232.1:g.34900G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.905G>C MANE Select ENSP00000416293.2:p.Gly302Ala
ENST00000674545.1:n.223G>C
ENST00000674765.1:c.905G>C ENSP00000501811.1:p.Gly302Ala
ENST00000675112.1:n.1206G>C
ENST00000676254.1:n.1354G>C
ENST00000426263.7:c.905G>C ENSP00000416293.2:p.Gly302Ala
ENST00000439722.2:c.784G>C ENSP00000395521.2:n.784G>C
ENST00000475162.3:c.415+1349G>C
ENST00000630287.2:c.*220G>C ENSP00000486694.1:n.*220G>C
NM_006516.2:c.905G>C NP_006507.2:p.Gly302Ala
NM_006516.3:c.905G>C NP_006507.2:p.Gly302Ala
NM_006516.4:c.905G>C MANE Select NP_006507.2:p.Gly302Ala