Canonical Allele Identifier: CA339958662
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929975T>A , CM000663.2:g.42929975T>A GRCh38
NC_000001.10:g.43395646T>A , CM000663.1:g.43395646T>A GRCh37
NC_000001.9:g.43168233T>A NCBI36
NG_008232.1:g.34202A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.577A>T MANE Select ENSP00000416293.2:p.Ile193Phe
ENST00000674765.1:c.577A>T ENSP00000501811.1:p.Ile193Phe
ENST00000675112.1:n.600A>T
ENST00000676254.1:n.1026A>T
ENST00000426263.7:c.577A>T ENSP00000416293.2:p.Ile193Phe
ENST00000439722.2:c.456A>T ENSP00000395521.2:n.456A>T
ENST00000475162.3:c.415+651A>T
ENST00000630287.2:c.517-195A>T ENSP00000486694.1:n.517-195A>T
NM_006516.2:c.577A>T NP_006507.2:p.Ile193Phe
NM_006516.3:c.577A>T NP_006507.2:p.Ile193Phe
NM_006516.4:c.577A>T MANE Select NP_006507.2:p.Ile193Phe