Canonical Allele Identifier: CA1165412774

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930730_42930732delinsCTG , CM000663.2:g.42930730_42930732delinsCTG	GRCh38
NC_000001.10:g.43396401_43396403delinsCTG , CM000663.1:g.43396401_43396403delinsCTG	GRCh37
NC_000001.9:g.43168988_43168990delinsCTG	NCBI36
NG_008232.1:g.33445_33447delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000426263.10:c.410_412delinsCAG MANE Select	ENSP00000416293.2:p.Thr137=
ENST00000674765.1:c.410_412delinsCAG	ENSP00000501811.1:p.Thr137=
ENST00000675112.1:n.433_435delinsCAG
ENST00000676254.1:n.859_861delinsCAG
ENST00000372500.4:c.314_316delinsCAG	ENSP00000361578.4:p.Thr105=
ENST00000426263.7:c.410_412delinsCAG	ENSP00000416293.2:p.Thr137=
ENST00000439722.2:c.289_291delinsCAG	ENSP00000395521.2:n.289_291delinsCAG
ENST00000475162.3:c.309_311delinsCAG
ENST00000625233.2:n.618_620delinsCAG
ENST00000630287.2:c.410_412delinsCAG	ENSP00000486694.1:p.Thr137=
NM_006516.2:c.410_412delinsCAG	NP_006507.2:p.Thr137=
NM_006516.3:c.410_412delinsCAG	NP_006507.2:p.Thr137=
NM_006516.4:c.410_412delinsCAG MANE Select	NP_006507.2:p.Thr137=