Canonical Allele Identifier: CA803383

Gene: SLC2A1

Linked Data

• dbSNP Id: rs767433467
• ExAC: 1:43394822 A / G
• gnomAD v2: 1-43394822-A-G
• gnomAD v4: 1-42929151-A-G
• MyVariant Identifiers: chr1:g.43394822A>G (hg19) ; chr1:g.42929151A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929151A>G , CM000663.2:g.42929151A>G	GRCh38
NC_000001.10:g.43394822A>G , CM000663.1:g.43394822A>G	GRCh37
NC_000001.9:g.43167409A>G	NCBI36
NG_008232.1:g.35026T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+59T>C MANE Select	ENSP00000416293.2:n.972+59T>C
ENST00000674545.1:n.349T>C
ENST00000674765.1:c.972+59T>C	ENSP00000501811.1:n.972+59T>C
ENST00000675112.1:n.1273+59T>C
ENST00000676254.1:n.1421+59T>C
ENST00000426263.7:c.972+59T>C	ENSP00000416293.2:n.972+59T>C
ENST00000439722.2:c.851+59T>C	ENSP00000395521.2:n.851+59T>C
ENST00000475162.3:c.415+1475T>C
ENST00000630287.2:c.*287+59T>C	ENSP00000486694.1:n.*287+59T>C
NM_006516.2:c.972+59T>C	NP_006507.2:n.972+59T>C
NM_006516.3:c.972+59T>C	NP_006507.2:n.972+59T>C
NM_006516.4:c.972+59T>C MANE Select	NP_006507.2:n.972+59T>C