Canonical Allele Identifier: CA339957738
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929677C>A , CM000663.2:g.42929677C>A GRCh38
NC_000001.10:g.43395348C>A , CM000663.1:g.43395348C>A GRCh37
NC_000001.9:g.43167935C>A NCBI36
NG_008232.1:g.34500G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.783G>T MANE Select ENSP00000416293.2:p.Glu261Asp
ENST00000669445.1:c.113G>T
ENST00000674765.1:c.783G>T ENSP00000501811.1:p.Glu261Asp
ENST00000675112.1:n.806G>T
ENST00000676254.1:n.1232G>T
ENST00000426263.7:c.783G>T ENSP00000416293.2:p.Glu261Asp
ENST00000439722.2:c.662G>T ENSP00000395521.2:n.662G>T
ENST00000475162.3:c.415+949G>T
ENST00000630287.2:c.*98G>T ENSP00000486694.1:n.*98G>T
NM_006516.2:c.783G>T NP_006507.2:p.Glu261Asp
NM_006516.3:c.783G>T NP_006507.2:p.Glu261Asp
NM_006516.4:c.783G>T MANE Select NP_006507.2:p.Glu261Asp