Canonical Allele Identifier: CA417409470

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43396300G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930629G>T , CM000663.2:g.42930629G>T	GRCh38
NC_000001.10:g.43396300G>T , CM000663.1:g.43396300G>T	GRCh37
NC_000001.9:g.43168887G>T	NCBI36
NG_008232.1:g.33548C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000426263.10:c.513C>A MANE Select	ENSP00000416293.2:p.Ala171=
ENST00000674765.1:c.513C>A	ENSP00000501811.1:p.Ala171=
ENST00000675112.1:n.536C>A
ENST00000676254.1:n.962C>A
ENST00000426263.7:c.513C>A	ENSP00000416293.2:p.Ala171=
ENST00000439722.2:c.392C>A	ENSP00000395521.2:n.392C>A
ENST00000475162.3:c.412C>A
ENST00000625233.2:n.721C>A
ENST00000630287.2:c.513C>A	ENSP00000486694.1:p.Ala171=
NM_006516.2:c.513C>A	NP_006507.2:p.Ala171=
NM_006516.3:c.513C>A	NP_006507.2:p.Ala171=
NM_006516.4:c.513C>A MANE Select	NP_006507.2:p.Ala171=