Canonical Allele Identifier: CA417409093

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43394935A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929264A>T , CM000663.2:g.42929264A>T	GRCh38
NC_000001.10:g.43394935A>T , CM000663.1:g.43394935A>T	GRCh37
NC_000001.9:g.43167522A>T	NCBI36
NG_008232.1:g.34913T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.918T>A MANE Select	ENSP00000416293.2:p.Pro306=
ENST00000674545.1:n.236T>A
ENST00000674765.1:c.918T>A	ENSP00000501811.1:p.Pro306=
ENST00000675112.1:n.1219T>A
ENST00000676254.1:n.1367T>A
ENST00000426263.7:c.918T>A	ENSP00000416293.2:p.Pro306=
ENST00000439722.2:c.797T>A	ENSP00000395521.2:n.797T>A
ENST00000475162.3:c.415+1362T>A
ENST00000630287.2:c.*233T>A	ENSP00000486694.1:n.*233T>A
NM_006516.2:c.918T>A	NP_006507.2:p.Pro306=
NM_006516.3:c.918T>A	NP_006507.2:p.Pro306=
NM_006516.4:c.918T>A MANE Select	NP_006507.2:p.Pro306=