Canonical Allele Identifier: CA339961329
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930837A>T , CM000663.2:g.42930837A>T GRCh38
NC_000001.10:g.43396508A>T , CM000663.1:g.43396508A>T GRCh37
NC_000001.9:g.43169095A>T NCBI36
NG_008232.1:g.33340T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.305T>A MANE Select ENSP00000416293.2:p.Leu102Gln
ENST00000674765.1:c.305T>A ENSP00000501811.1:p.Leu102Gln
ENST00000675112.1:n.328T>A
ENST00000676254.1:n.754T>A
ENST00000372500.4:c.209T>A ENSP00000361578.4:p.Leu70Gln
ENST00000426263.7:c.305T>A ENSP00000416293.2:p.Leu102Gln
ENST00000439722.2:c.184T>A ENSP00000395521.2:n.184T>A
ENST00000475162.3:c.204T>A
ENST00000625233.2:n.513T>A
ENST00000630287.2:c.305T>A ENSP00000486694.1:p.Leu102Gln
NM_006516.2:c.305T>A NP_006507.2:p.Leu102Gln
NM_006516.3:c.305T>A NP_006507.2:p.Leu102Gln
NM_006516.4:c.305T>A MANE Select NP_006507.2:p.Leu102Gln