Canonical Allele Identifier: CA339958135
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929738A>T , CM000663.2:g.42929738A>T GRCh38
NC_000001.10:g.43395409A>T , CM000663.1:g.43395409A>T GRCh37
NC_000001.9:g.43167996A>T NCBI36
NG_008232.1:g.34439T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.722T>A MANE Select ENSP00000416293.2:p.Leu241Gln
ENST00000669445.1:c.57-5T>A
ENST00000674765.1:c.722T>A ENSP00000501811.1:p.Leu241Gln
ENST00000675112.1:n.745T>A
ENST00000676254.1:n.1171T>A
ENST00000426263.7:c.722T>A ENSP00000416293.2:p.Leu241Gln
ENST00000439722.2:c.601T>A ENSP00000395521.2:n.601T>A
ENST00000475162.3:c.415+888T>A
ENST00000630287.2:c.*37T>A ENSP00000486694.1:n.*37T>A
NM_006516.2:c.722T>A NP_006507.2:p.Leu241Gln
NM_006516.3:c.722T>A NP_006507.2:p.Leu241Gln
NM_006516.4:c.722T>A MANE Select NP_006507.2:p.Leu241Gln