Canonical Allele Identifier: CA339954113
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927750A>G , CM000663.2:g.42927750A>G GRCh38
NC_000001.10:g.43393421A>G , CM000663.1:g.43393421A>G GRCh37
NC_000001.9:g.43166008A>G NCBI36
NG_008232.1:g.36427T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1133T>C MANE Select ENSP00000416293.2:p.Phe378Ser
ENST00000674545.1:n.1750T>C
ENST00000674765.1:c.1030-893T>C ENSP00000501811.1:n.1030-893T>C
ENST00000675112.1:n.1434T>C
ENST00000676254.1:n.1582T>C
ENST00000426263.7:c.1133T>C ENSP00000416293.2:p.Phe378Ser
ENST00000475162.3:c.416-772T>C
ENST00000630287.2:c.*448T>C ENSP00000486694.1:n.*448T>C
NM_006516.2:c.1133T>C NP_006507.2:p.Phe378Ser
NM_006516.3:c.1133T>C NP_006507.2:p.Phe378Ser
NM_006516.4:c.1133T>C MANE Select NP_006507.2:p.Phe378Ser