Canonical Allele Identifier: CA417543718

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396366G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930695G>T , CM000663.2:g.42930695G>T	GRCh38
NC_000001.10:g.43396366G>T , CM000663.1:g.43396366G>T	GRCh37
NC_000001.9:g.43168953G>T	NCBI36
NG_008232.1:g.33482C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.447C>A MANE Select	ENSP00000416293.2:p.Pro149=
ENST00000674765.1:c.447C>A	ENSP00000501811.1:p.Pro149=
ENST00000675112.1:n.470C>A
ENST00000676254.1:n.896C>A
ENST00000426263.7:c.447C>A	ENSP00000416293.2:p.Pro149=
ENST00000439722.2:c.326C>A	ENSP00000395521.2:n.326C>A
ENST00000475162.3:c.346C>A
ENST00000625233.2:n.655C>A
ENST00000630287.2:c.447C>A	ENSP00000486694.1:p.Pro149=
NM_006516.2:c.447C>A	NP_006507.2:p.Pro149=
NM_006516.3:c.447C>A	NP_006507.2:p.Pro149=
NM_006516.4:c.447C>A MANE Select	NP_006507.2:p.Pro149=