Canonical Allele Identifier: CA1165417879
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42943534_42943535delinsTG , CM000663.2:g.42943534_42943535delinsTG GRCh38
NC_000001.10:g.43409205_43409206delinsTG , CM000663.1:g.43409205_43409206delinsTG GRCh37
NC_000001.9:g.43181792_43181793delinsTG NCBI36
NG_008232.1:g.20642_20643delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.19-214_19-213delinsCA MANE Select ENSP00000416293.2:n.19-214_19-213delinsCA
ENST00000674765.1:c.19-214_19-213delinsCA ENSP00000501811.1:n.19-214_19-213delinsCA
ENST00000675112.1:n.42-214_42-213delinsCA
ENST00000372500.4:c.19-12329_19-12328delinsCA ENSP00000361578.4:n.19-12329_19-12328delinsCA
ENST00000415851.6:n.236-214_236-213delinsCA
ENST00000426263.7:c.19-214_19-213delinsCA ENSP00000416293.2:n.19-214_19-213delinsCA
ENST00000625233.2:n.227-214_227-213delinsCA
ENST00000628173.1:n.238-214_238-213delinsCA
ENST00000630287.2:c.19-214_19-213delinsCA ENSP00000486694.1:n.19-214_19-213delinsCA
ENST00000630821.1:n.236-214_236-213delinsCA
NM_006516.2:c.19-214_19-213delinsCA NP_006507.2:n.19-214_19-213delinsCA
NM_006516.3:c.19-214_19-213delinsCA NP_006507.2:n.19-214_19-213delinsCA
NM_006516.4:c.19-214_19-213delinsCA MANE Select NP_006507.2:n.19-214_19-213delinsCA