Canonical Allele Identifier: CA339957834
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929687G>A , CM000663.2:g.42929687G>A GRCh38
NC_000001.10:g.43395358G>A , CM000663.1:g.43395358G>A GRCh37
NC_000001.9:g.43167945G>A NCBI36
NG_008232.1:g.34490C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.773C>T MANE Select ENSP00000416293.2:p.Thr258Ile
ENST00000669445.1:c.103C>T
ENST00000674765.1:c.773C>T ENSP00000501811.1:p.Thr258Ile
ENST00000675112.1:n.796C>T
ENST00000676254.1:n.1222C>T
ENST00000426263.7:c.773C>T ENSP00000416293.2:p.Thr258Ile
ENST00000439722.2:c.652C>T ENSP00000395521.2:n.652C>T
ENST00000475162.3:c.415+939C>T
ENST00000630287.2:c.*88C>T ENSP00000486694.1:n.*88C>T
NM_006516.2:c.773C>T NP_006507.2:p.Thr258Ile
NM_006516.3:c.773C>T NP_006507.2:p.Thr258Ile
NM_006516.4:c.773C>T MANE Select NP_006507.2:p.Thr258Ile