Canonical Allele Identifier: CA339960197
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930634T>A , CM000663.2:g.42930634T>A GRCh38
NC_000001.10:g.43396305T>A , CM000663.1:g.43396305T>A GRCh37
NC_000001.9:g.43168892T>A NCBI36
NG_008232.1:g.33543A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.508A>T MANE Select ENSP00000416293.2:p.Ile170Phe
ENST00000674765.1:c.508A>T ENSP00000501811.1:p.Ile170Phe
ENST00000675112.1:n.531A>T
ENST00000676254.1:n.957A>T
ENST00000426263.7:c.508A>T ENSP00000416293.2:p.Ile170Phe
ENST00000439722.2:c.387A>T ENSP00000395521.2:n.387A>T
ENST00000475162.3:c.407A>T
ENST00000625233.2:n.716A>T
ENST00000630287.2:c.508A>T ENSP00000486694.1:p.Ile170Phe
NM_006516.2:c.508A>T NP_006507.2:p.Ile170Phe
NM_006516.3:c.508A>T NP_006507.2:p.Ile170Phe
NM_006516.4:c.508A>T MANE Select NP_006507.2:p.Ile170Phe