Canonical Allele Identifier: CA21249165
Gene: SLC2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304066
ClinVar RCV Id: RCV001751833 RCV002539910 RCV003389073 RCV003446885 RCV003446888 RCV003446886 RCV003446887
dbSNP Id: rs1027810691
gnomAD v2: 1-43393362-C-T
gnomAD v3: 1-42927691-C-T
gnomAD v4: 1-42927691-C-T
MyVariant Identifiers: chr1:g.43393362C>T (hg19) chr1:g.42927691C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927691C>T , CM000663.2:g.42927691C>T GRCh38
NC_000001.10:g.43393362C>T , CM000663.1:g.43393362C>T GRCh37
NC_000001.9:g.43165949C>T NCBI36
NG_008232.1:g.36486G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1192G>A MANE Select ENSP00000416293.2:p.Gly398Ser
ENST00000674545.1:n.1809G>A
ENST00000674765.1:c.1030-834G>A ENSP00000501811.1:n.1030-834G>A
ENST00000675112.1:n.1493G>A
ENST00000676254.1:n.1641G>A
ENST00000426263.7:c.1192G>A ENSP00000416293.2:p.Gly398Ser
ENST00000475162.3:c.416-713G>A
ENST00000630287.2:c.*507G>A ENSP00000486694.1:n.*507G>A
NM_006516.2:c.1192G>A NP_006507.2:p.Gly398Ser
NM_006516.3:c.1192G>A NP_006507.2:p.Gly398Ser
NM_006516.4:c.1192G>A MANE Select NP_006507.2:p.Gly398Ser
Search 100 bp 5'
Search 100 bp 3'