Canonical Allele Identifier: CA2691006237
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429843del , CM000671.2:g.101429843del GRCh38
NC_000009.11:g.104192125del , CM000671.1:g.104192125del GRCh37
NC_000009.10:g.103231946del NCBI36
NG_012387.1:g.10941del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.239del MANE Select ENSP00000497767.1:p.Phe80SerfsTer30
ENST00000648064.1:c.239del ENSP00000497990.1:p.Phe80SerfsTer30
ENST00000648758.1:c.239del ENSP00000497731.1:p.Phe80SerfsTer30
ENST00000648906.1:n.409del
ENST00000649902.1:c.239del ENSP00000497216.1:p.Phe80SerfsTer30
ENST00000650613.1:n.315del
ENST00000374855.8:c.239del ENSP00000363988.4:p.Phe80SerfsTer30
ENST00000468981.3:n.36del
ENST00000616752.1:c.239del ENSP00000481363.1:p.Phe80SerfsTer30
NM_000035.3:c.239del NP_000026.2:p.Phe80SerfsTer30
NM_000035.4:c.239del MANE Select NP_000026.2:p.Phe80SerfsTer30