Canonical Allele Identifier: CA417543392

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43395348C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929677C>T , CM000663.2:g.42929677C>T	GRCh38
NC_000001.10:g.43395348C>T , CM000663.1:g.43395348C>T	GRCh37
NC_000001.9:g.43167935C>T	NCBI36
NG_008232.1:g.34500G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.783G>A MANE Select	ENSP00000416293.2:p.Glu261=
ENST00000669445.1:c.113G>A
ENST00000674765.1:c.783G>A	ENSP00000501811.1:p.Glu261=
ENST00000675112.1:n.806G>A
ENST00000676254.1:n.1232G>A
ENST00000426263.7:c.783G>A	ENSP00000416293.2:p.Glu261=
ENST00000439722.2:c.662G>A	ENSP00000395521.2:n.662G>A
ENST00000475162.3:c.415+949G>A
ENST00000630287.2:c.*98G>A	ENSP00000486694.1:n.*98G>A
NM_006516.2:c.783G>A	NP_006507.2:p.Glu261=
NM_006516.3:c.783G>A	NP_006507.2:p.Glu261=
NM_006516.4:c.783G>A MANE Select	NP_006507.2:p.Glu261=