Canonical Allele Identifier: CA339956338

Gene: SLC2A1

Linked Data

• ClinVar Variation Id: 1321286
• ClinVar RCV Id: RCV001779387
• dbSNP Id: rs2124448276
• MyVariant Identifiers: chr1:g.43394892T>G (hg19) ; chr1:g.42929221T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929221T>G , CM000663.2:g.42929221T>G	GRCh38
NC_000001.10:g.43394892T>G , CM000663.1:g.43394892T>G	GRCh37
NC_000001.9:g.43167479T>G	NCBI36
NG_008232.1:g.34956A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.961A>C MANE Select	ENSP00000416293.2:p.Thr321Pro
ENST00000674545.1:n.279A>C
ENST00000674765.1:c.961A>C	ENSP00000501811.1:p.Thr321Pro
ENST00000675112.1:n.1262A>C
ENST00000676254.1:n.1410A>C
ENST00000426263.7:c.961A>C	ENSP00000416293.2:p.Thr321Pro
ENST00000439722.2:c.840A>C	ENSP00000395521.2:n.840A>C
ENST00000475162.3:c.415+1405A>C
ENST00000630287.2:c.*276A>C	ENSP00000486694.1:n.*276A>C
NM_006516.2:c.961A>C	NP_006507.2:p.Thr321Pro
NM_006516.3:c.961A>C	NP_006507.2:p.Thr321Pro
NM_006516.4:c.961A>C MANE Select	NP_006507.2:p.Thr321Pro