Canonical Allele Identifier: CA10670028
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs841847
gnomAD v2: 1-43402708-T-C
gnomAD v3: 1-42937037-T-C
gnomAD v4: 1-42937037-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42937037T>C , CM000663.2:g.42937037T>C GRCh38
NC_000001.10:g.43402708T>C , CM000663.1:g.43402708T>C GRCh37
NC_000001.9:g.43175295T>C NCBI36
NG_008232.1:g.27140A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.115-5831A>G MANE Select ENSP00000416293.2:n.115-5831A>G
ENST00000674765.1:c.115-5831A>G ENSP00000501811.1:n.115-5831A>G
ENST00000675112.1:n.138-5831A>G
ENST00000372500.4:c.19-5831A>G ENSP00000361578.4:n.19-5831A>G
ENST00000415851.6:n.332-5831A>G
ENST00000426263.7:c.115-5831A>G ENSP00000416293.2:n.115-5831A>G
ENST00000475162.3:c.14-5831A>G
ENST00000625233.2:n.323-5831A>G
ENST00000628173.1:n.460+2786A>G
ENST00000630287.2:c.115-5831A>G ENSP00000486694.1:n.115-5831A>G
NM_006516.2:c.115-5831A>G NP_006507.2:n.115-5831A>G
NM_006516.3:c.115-5831A>G NP_006507.2:n.115-5831A>G
NM_006516.4:c.115-5831A>G MANE Select NP_006507.2:n.115-5831A>G