Canonical Allele Identifier: CA339958175
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929748T>G , CM000663.2:g.42929748T>G GRCh38
NC_000001.10:g.43395419T>G , CM000663.1:g.43395419T>G GRCh37
NC_000001.9:g.43168006T>G NCBI36
NG_008232.1:g.34429A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.712A>C MANE Select ENSP00000416293.2:p.Thr238Pro
ENST00000669445.1:c.57-15A>C
ENST00000674765.1:c.712A>C ENSP00000501811.1:p.Thr238Pro
ENST00000675112.1:n.735A>C
ENST00000676254.1:n.1161A>C
ENST00000426263.7:c.712A>C ENSP00000416293.2:p.Thr238Pro
ENST00000439722.2:c.591A>C ENSP00000395521.2:n.591A>C
ENST00000475162.3:c.415+878A>C
ENST00000630287.2:c.*27A>C ENSP00000486694.1:n.*27A>C
NM_006516.2:c.712A>C NP_006507.2:p.Thr238Pro
NM_006516.3:c.712A>C NP_006507.2:p.Thr238Pro
NM_006516.4:c.712A>C MANE Select NP_006507.2:p.Thr238Pro