Canonical Allele Identifier: CA2691007538
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427625del , CM000671.2:g.101427625del GRCh38
NC_000009.11:g.104189907del , CM000671.1:g.104189907del GRCh37
NC_000009.10:g.103229728del NCBI36
NG_012387.1:g.13156del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.397del MANE Select ENSP00000497767.1:p.Glu133SerfsTer20
ENST00000648064.1:c.397del ENSP00000497990.1:p.Glu133SerfsTer20
ENST00000648758.1:c.397del ENSP00000497731.1:p.Glu133SerfsTer20
ENST00000649902.1:c.397del ENSP00000497216.1:p.Glu133SerfsTer20
ENST00000374855.8:c.397del ENSP00000363988.4:p.Glu133SerfsTer20
ENST00000468981.3:n.68-987del
ENST00000616752.1:c.397del ENSP00000481363.1:p.Glu133SerfsTer20
NM_000035.3:c.397del NP_000026.2:p.Glu133SerfsTer20
NM_000035.4:c.397del MANE Select NP_000026.2:p.Glu133SerfsTer20