Canonical Allele Identifier: CA339960507
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930675A>T , CM000663.2:g.42930675A>T GRCh38
NC_000001.10:g.43396346A>T , CM000663.1:g.43396346A>T GRCh37
NC_000001.9:g.43168933A>T NCBI36
NG_008232.1:g.33502T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.467T>A MANE Select ENSP00000416293.2:p.Leu156Gln
ENST00000674765.1:c.467T>A ENSP00000501811.1:p.Leu156Gln
ENST00000675112.1:n.490T>A
ENST00000676254.1:n.916T>A
ENST00000426263.7:c.467T>A ENSP00000416293.2:p.Leu156Gln
ENST00000439722.2:c.346T>A ENSP00000395521.2:n.346T>A
ENST00000475162.3:c.366T>A
ENST00000625233.2:n.675T>A
ENST00000630287.2:c.467T>A ENSP00000486694.1:p.Leu156Gln
NM_006516.2:c.467T>A NP_006507.2:p.Leu156Gln
NM_006516.3:c.467T>A NP_006507.2:p.Leu156Gln
NM_006516.4:c.467T>A MANE Select NP_006507.2:p.Leu156Gln