Canonical Allele Identifier: CA2645199329
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42929842-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929842A>C , CM000663.2:g.42929842A>C GRCh38
NC_000001.10:g.43395513A>C , CM000663.1:g.43395513A>C GRCh37
NC_000001.9:g.43168100A>C NCBI36
NG_008232.1:g.34335T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.679+31T>G MANE Select ENSP00000416293.2:n.679+31T>G
ENST00000669445.1:c.56+31T>G
ENST00000674765.1:c.679+31T>G ENSP00000501811.1:n.679+31T>G
ENST00000675112.1:n.702+31T>G
ENST00000676254.1:n.1128+31T>G
ENST00000426263.7:c.679+31T>G ENSP00000416293.2:n.679+31T>G
ENST00000439722.2:c.558+31T>G ENSP00000395521.2:n.558+31T>G
ENST00000475162.3:c.415+784T>G
ENST00000630287.2:c.517-62T>G ENSP00000486694.1:n.517-62T>G
NM_006516.2:c.679+31T>G NP_006507.2:n.679+31T>G
NM_006516.3:c.679+31T>G NP_006507.2:n.679+31T>G
NM_006516.4:c.679+31T>G MANE Select NP_006507.2:n.679+31T>G