Canonical Allele Identifier: CA2645199365
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42943179-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943179A>C , CM000663.2:g.42943179A>C GRCh38
NC_000001.10:g.43408850A>C , CM000663.1:g.43408850A>C GRCh37
NC_000001.9:g.43181437A>C NCBI36
NG_008232.1:g.20998T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.114+47T>G MANE Select ENSP00000416293.2:n.114+47T>G
ENST00000674765.1:c.114+47T>G ENSP00000501811.1:n.114+47T>G
ENST00000675112.1:n.137+47T>G
ENST00000372500.4:c.19-11973T>G ENSP00000361578.4:n.19-11973T>G
ENST00000415851.6:n.331+47T>G
ENST00000426263.7:c.114+47T>G ENSP00000416293.2:n.114+47T>G
ENST00000475162.3:c.13+47T>G
ENST00000625233.2:n.322+47T>G
ENST00000628173.1:n.333+47T>G
ENST00000630287.2:c.114+47T>G ENSP00000486694.1:n.114+47T>G
ENST00000630821.1:n.378T>G
NM_006516.2:c.114+47T>G NP_006507.2:n.114+47T>G
NM_006516.3:c.114+47T>G NP_006507.2:n.114+47T>G
NM_006516.4:c.114+47T>G MANE Select NP_006507.2:n.114+47T>G