Canonical Allele Identifier: CA2739272509

Gene: SLC2A1

Linked Data

• ClinVar Variation Id: 2832634
• ClinVar RCV Id: RCV003631883

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930607A>T , CM000663.2:g.42930607A>T	GRCh38
NC_000001.10:g.43396278A>T , CM000663.1:g.43396278A>T	GRCh37
NC_000001.9:g.43168865A>T	NCBI36
NG_008232.1:g.33570T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.516+19T>A MANE Select	ENSP00000416293.2:n.516+19T>A
ENST00000674765.1:c.516+19T>A	ENSP00000501811.1:n.516+19T>A
ENST00000675112.1:n.539+19T>A
ENST00000676254.1:n.965+19T>A
ENST00000426263.7:c.516+19T>A	ENSP00000416293.2:n.516+19T>A
ENST00000439722.2:c.395+19T>A	ENSP00000395521.2:n.395+19T>A
ENST00000475162.3:c.415+19T>A
ENST00000625233.2:n.743T>A
ENST00000630287.2:c.516+19T>A	ENSP00000486694.1:n.516+19T>A
NM_006516.2:c.516+19T>A	NP_006507.2:n.516+19T>A
NM_006516.3:c.516+19T>A	NP_006507.2:n.516+19T>A
NM_006516.4:c.516+19T>A MANE Select	NP_006507.2:n.516+19T>A