Canonical Allele Identifier: CA339958463
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929878T>G , CM000663.2:g.42929878T>G GRCh38
NC_000001.10:g.43395549T>G , CM000663.1:g.43395549T>G GRCh37
NC_000001.9:g.43168136T>G NCBI36
NG_008232.1:g.34299A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.674A>C MANE Select ENSP00000416293.2:p.Lys225Thr
ENST00000669445.1:c.51A>C
ENST00000674765.1:c.674A>C ENSP00000501811.1:p.Lys225Thr
ENST00000675112.1:n.697A>C
ENST00000676254.1:n.1123A>C
ENST00000426263.7:c.674A>C ENSP00000416293.2:p.Lys225Thr
ENST00000439722.2:c.553A>C ENSP00000395521.2:n.553A>C
ENST00000475162.3:c.415+748A>C
ENST00000630287.2:c.517-98A>C ENSP00000486694.1:n.517-98A>C
NM_006516.2:c.674A>C NP_006507.2:p.Lys225Thr
NM_006516.3:c.674A>C NP_006507.2:p.Lys225Thr
NM_006516.4:c.674A>C MANE Select NP_006507.2:p.Lys225Thr