Canonical Allele Identifier: CA417409027

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43394911A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929240A>C , CM000663.2:g.42929240A>C	GRCh38
NC_000001.10:g.43394911A>C , CM000663.1:g.43394911A>C	GRCh37
NC_000001.9:g.43167498A>C	NCBI36
NG_008232.1:g.34937T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.942T>G MANE Select	ENSP00000416293.2:p.Gly314=
ENST00000674545.1:n.260T>G
ENST00000674765.1:c.942T>G	ENSP00000501811.1:p.Gly314=
ENST00000675112.1:n.1243T>G
ENST00000676254.1:n.1391T>G
ENST00000426263.7:c.942T>G	ENSP00000416293.2:p.Gly314=
ENST00000439722.2:c.821T>G	ENSP00000395521.2:n.821T>G
ENST00000475162.3:c.415+1386T>G
ENST00000630287.2:c.*257T>G	ENSP00000486694.1:n.*257T>G
NM_006516.2:c.942T>G	NP_006507.2:p.Gly314=
NM_006516.3:c.942T>G	NP_006507.2:p.Gly314=
NM_006516.4:c.942T>G MANE Select	NP_006507.2:p.Gly314=