Canonical Allele Identifier: CA803413

Gene: SLC2A1

Linked Data

• dbSNP Id: rs754313587
• ExAC: 1:43395037 C / T
• gnomAD v2: 1-43395037-C-T
• gnomAD v3: 1-42929366-C-T
• gnomAD v4: 1-42929366-C-T
• MyVariant Identifiers: chr1:g.43395037C>T (hg19) ; chr1:g.42929366C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929366C>T , CM000663.2:g.42929366C>T	GRCh38
NC_000001.10:g.43395037C>T , CM000663.1:g.43395037C>T	GRCh37
NC_000001.9:g.43167624C>T	NCBI36
NG_008232.1:g.34811G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.868-52G>A MANE Select	ENSP00000416293.2:n.868-52G>A
ENST00000674545.1:n.134G>A
ENST00000674765.1:c.868-52G>A	ENSP00000501811.1:n.868-52G>A
ENST00000675112.1:n.1117G>A
ENST00000676254.1:n.1317-52G>A
ENST00000426263.7:c.868-52G>A	ENSP00000416293.2:n.868-52G>A
ENST00000439722.2:c.747-52G>A	ENSP00000395521.2:n.747-52G>A
ENST00000475162.3:c.415+1260G>A
ENST00000630287.2:c.*183-52G>A	ENSP00000486694.1:n.*183-52G>A
NM_006516.2:c.868-52G>A	NP_006507.2:n.868-52G>A
NM_006516.3:c.868-52G>A	NP_006507.2:n.868-52G>A
NM_006516.4:c.868-52G>A MANE Select	NP_006507.2:n.868-52G>A