Canonical Allele Identifier: CA1001056326
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1643619823
gnomAD v3: 1-42943538-G-A
gnomAD v4: 1-42943538-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943538G>A , CM000663.2:g.42943538G>A GRCh38
NC_000001.10:g.43409209G>A , CM000663.1:g.43409209G>A GRCh37
NC_000001.9:g.43181796G>A NCBI36
NG_008232.1:g.20639C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-217C>T MANE Select ENSP00000416293.2:n.19-217C>T
ENST00000674765.1:c.19-217C>T ENSP00000501811.1:n.19-217C>T
ENST00000675112.1:n.42-217C>T
ENST00000372500.4:c.19-12332C>T ENSP00000361578.4:n.19-12332C>T
ENST00000415851.6:n.236-217C>T
ENST00000426263.7:c.19-217C>T ENSP00000416293.2:n.19-217C>T
ENST00000625233.2:n.227-217C>T
ENST00000628173.1:n.238-217C>T
ENST00000630287.2:c.19-217C>T ENSP00000486694.1:n.19-217C>T
ENST00000630821.1:n.236-217C>T
NM_006516.2:c.19-217C>T NP_006507.2:n.19-217C>T
NM_006516.3:c.19-217C>T NP_006507.2:n.19-217C>T
NM_006516.4:c.19-217C>T MANE Select NP_006507.2:n.19-217C>T