Canonical Allele Identifier: CA417408061

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43394603C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42928932C>T , CM000663.2:g.42928932C>T	GRCh38
NC_000001.10:g.43394603C>T , CM000663.1:g.43394603C>T	GRCh37
NC_000001.9:g.43167190C>T	NCBI36
NG_008232.1:g.35245G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1074G>A MANE Select	ENSP00000416293.2:p.Leu358=
ENST00000674545.1:n.568G>A
ENST00000674765.1:c.1029+45G>A	ENSP00000501811.1:n.1029+45G>A
ENST00000675112.1:n.1375G>A
ENST00000676254.1:n.1523G>A
ENST00000426263.7:c.1074G>A	ENSP00000416293.2:p.Leu358=
ENST00000475162.3:c.415+1694G>A
ENST00000630287.2:c.*389G>A	ENSP00000486694.1:n.*389G>A
NM_006516.2:c.1074G>A	NP_006507.2:p.Leu358=
NM_006516.3:c.1074G>A	NP_006507.2:p.Leu358=
NM_006516.4:c.1074G>A MANE Select	NP_006507.2:p.Leu358=