Canonical Allele Identifier: CA339960486

Gene: SLC2A1

Linked Data

• ClinVar Variation Id: 436753
• ClinVar RCV Id: RCV000503688
• dbSNP Id: rs1553156155
• MyVariant Identifiers: chr1:g.43396341T>G (hg19) ; chr1:g.42930670T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930670T>G , CM000663.2:g.42930670T>G	GRCh38
NC_000001.10:g.43396341T>G , CM000663.1:g.43396341T>G	GRCh37
NC_000001.9:g.43168928T>G	NCBI36
NG_008232.1:g.33507A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.472A>C MANE Select	ENSP00000416293.2:p.Thr158Pro
ENST00000674765.1:c.472A>C	ENSP00000501811.1:p.Thr158Pro
ENST00000675112.1:n.495A>C
ENST00000676254.1:n.921A>C
ENST00000426263.7:c.472A>C	ENSP00000416293.2:p.Thr158Pro
ENST00000439722.2:c.351A>C	ENSP00000395521.2:n.351A>C
ENST00000475162.3:c.371A>C
ENST00000625233.2:n.680A>C
ENST00000630287.2:c.472A>C	ENSP00000486694.1:p.Thr158Pro
NM_006516.2:c.472A>C	NP_006507.2:p.Thr158Pro
NM_006516.3:c.472A>C	NP_006507.2:p.Thr158Pro
NM_006516.4:c.472A>C MANE Select	NP_006507.2:p.Thr158Pro