Canonical Allele Identifier: CA339956658
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929258A>C , CM000663.2:g.42929258A>C GRCh38
NC_000001.10:g.43394929A>C , CM000663.1:g.43394929A>C GRCh37
NC_000001.9:g.43167516A>C NCBI36
NG_008232.1:g.34919T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.924T>G MANE Select ENSP00000416293.2:p.Tyr308Ter
ENST00000674545.1:n.242T>G
ENST00000674765.1:c.924T>G ENSP00000501811.1:p.Tyr308Ter
ENST00000675112.1:n.1225T>G
ENST00000676254.1:n.1373T>G
ENST00000426263.7:c.924T>G ENSP00000416293.2:p.Tyr308Ter
ENST00000439722.2:c.803T>G ENSP00000395521.2:n.803T>G
ENST00000475162.3:c.415+1368T>G
ENST00000630287.2:c.*239T>G ENSP00000486694.1:n.*239T>G
NM_006516.2:c.924T>G NP_006507.2:p.Tyr308Ter
NM_006516.3:c.924T>G NP_006507.2:p.Tyr308Ter
NM_006516.4:c.924T>G MANE Select NP_006507.2:p.Tyr308Ter