Canonical Allele Identifier: CA2691006599
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101430678del , CM000671.2:g.101430678del GRCh38
NC_000009.11:g.104192960del , CM000671.1:g.104192960del GRCh37
NC_000009.10:g.103232781del NCBI36
NG_012387.1:g.10105del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.112+100del MANE Select ENSP00000497767.1:n.112+100del
ENST00000648064.1:c.112+100del ENSP00000497990.1:n.112+100del
ENST00000648423.1:c.112+100del ENSP00000497985.1:n.112+100del
ENST00000648758.1:c.112+100del ENSP00000497731.1:n.112+100del
ENST00000648906.1:n.282+100del
ENST00000649902.1:c.112+100del ENSP00000497216.1:n.112+100del
ENST00000650613.1:n.188+100del
ENST00000374855.8:c.112+100del ENSP00000363988.4:n.112+100del
ENST00000616752.1:c.112+100del ENSP00000481363.1:n.112+100del
NM_000035.3:c.112+100del NP_000026.2:n.112+100del
NM_000035.4:c.112+100del MANE Select NP_000026.2:n.112+100del