Canonical Allele Identifier: CA2695702992

Gene: SLC2A1

Linked Data

• dbSNP Id: rs2124446609

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927809_42927810insAGCAG , CM000663.2:g.42927809_42927810insAGCAG	GRCh38
NC_000001.10:g.43393480_43393481insAGCAG , CM000663.1:g.43393480_43393481insAGCAG	GRCh37
NC_000001.9:g.43166067_43166068insAGCAG	NCBI36
NG_008232.1:g.36367_36368insCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1075-2_1075-1insCTGCT MANE Select	ENSP00000416293.2:n.1075-2_1075-1insCTGCT
ENST00000674545.1:n.1690_1691insCTGCT
ENST00000674765.1:c.1030-953_1030-952insCTGCT	ENSP00000501811.1:n.1030-953_1030-952insCTGCT
ENST00000675112.1:n.1376-2_1376-1insCTGCT
ENST00000676254.1:n.1524-2_1524-1insCTGCT
ENST00000426263.7:c.1075-2_1075-1insCTGCT	ENSP00000416293.2:n.1075-2_1075-1insCTGCT
ENST00000475162.3:c.416-832_416-831insCTGCT
ENST00000630287.2:c.*390-2_*390-1insCTGCT	ENSP00000486694.1:n.*390-2_*390-1insCTGCT
NM_006516.2:c.1075-2_1075-1insCTGCT	NP_006507.2:n.1075-2_1075-1insCTGCT
NM_006516.3:c.1075-2_1075-1insCTGCT	NP_006507.2:n.1075-2_1075-1insCTGCT
NM_006516.4:c.1075-2_1075-1insCTGCT MANE Select	NP_006507.2:n.1075-2_1075-1insCTGCT