Canonical Allele Identifier: CA417409522

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396312G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930641G>T , CM000663.2:g.42930641G>T	GRCh38
NC_000001.10:g.43396312G>T , CM000663.1:g.43396312G>T	GRCh37
NC_000001.9:g.43168899G>T	NCBI36
NG_008232.1:g.33536C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.501C>A MANE Select	ENSP00000416293.2:p.Gly167=
ENST00000674765.1:c.501C>A	ENSP00000501811.1:p.Gly167=
ENST00000675112.1:n.524C>A
ENST00000676254.1:n.950C>A
ENST00000426263.7:c.501C>A	ENSP00000416293.2:p.Gly167=
ENST00000439722.2:c.380C>A	ENSP00000395521.2:n.380C>A
ENST00000475162.3:c.400C>A
ENST00000625233.2:n.709C>A
ENST00000630287.2:c.501C>A	ENSP00000486694.1:p.Gly167=
NM_006516.2:c.501C>A	NP_006507.2:p.Gly167=
NM_006516.3:c.501C>A	NP_006507.2:p.Gly167=
NM_006516.4:c.501C>A MANE Select	NP_006507.2:p.Gly167=