Canonical Allele Identifier: CA2645199430
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42943406-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943406T>C , CM000663.2:g.42943406T>C GRCh38
NC_000001.10:g.43409077T>C , CM000663.1:g.43409077T>C GRCh37
NC_000001.9:g.43181664T>C NCBI36
NG_008232.1:g.20771A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-85A>G MANE Select ENSP00000416293.2:n.19-85A>G
ENST00000674765.1:c.19-85A>G ENSP00000501811.1:n.19-85A>G
ENST00000675112.1:n.42-85A>G
ENST00000372500.4:c.19-12200A>G ENSP00000361578.4:n.19-12200A>G
ENST00000415851.6:n.236-85A>G
ENST00000426263.7:c.19-85A>G ENSP00000416293.2:n.19-85A>G
ENST00000625233.2:n.227-85A>G
ENST00000628173.1:n.238-85A>G
ENST00000630287.2:c.19-85A>G ENSP00000486694.1:n.19-85A>G
ENST00000630821.1:n.236-85A>G
NM_006516.2:c.19-85A>G NP_006507.2:n.19-85A>G
NM_006516.3:c.19-85A>G NP_006507.2:n.19-85A>G
NM_006516.4:c.19-85A>G MANE Select NP_006507.2:n.19-85A>G