Canonical Allele Identifier: CA16610098

Gene: SLC2A1

Linked Data

• ClinVar Variation Id: 406882
• ClinVar RCV Id: RCV000470279
• dbSNP Id: rs1060501354
• MyVariant Identifiers: chr1:g.43394888A>G (hg19) ; chr1:g.42929217A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929217A>G , CM000663.2:g.42929217A>G	GRCh38
NC_000001.10:g.43394888A>G , CM000663.1:g.43394888A>G	GRCh37
NC_000001.9:g.43167475A>G	NCBI36
NG_008232.1:g.34960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.965T>C MANE Select	ENSP00000416293.2:p.Val322Ala
ENST00000674545.1:n.283T>C
ENST00000674765.1:c.965T>C	ENSP00000501811.1:p.Val322Ala
ENST00000675112.1:n.1266T>C
ENST00000676254.1:n.1414T>C
ENST00000426263.7:c.965T>C	ENSP00000416293.2:p.Val322Ala
ENST00000439722.2:c.844T>C	ENSP00000395521.2:n.844T>C
ENST00000475162.3:c.415+1409T>C
ENST00000630287.2:c.*280T>C	ENSP00000486694.1:n.*280T>C
NM_006516.2:c.965T>C	NP_006507.2:p.Val322Ala
NM_006516.3:c.965T>C	NP_006507.2:p.Val322Ala
NM_006516.4:c.965T>C MANE Select	NP_006507.2:p.Val322Ala