Canonical Allele Identifier: CA2579403767
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101430723del , CM000671.2:g.101430723del GRCh38
NC_000009.11:g.104193005del , CM000671.1:g.104193005del GRCh37
NC_000009.10:g.103232826del NCBI36
NG_012387.1:g.10059del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.112+54del MANE Select ENSP00000497767.1:n.112+54del
ENST00000648064.1:c.112+54del ENSP00000497990.1:n.112+54del
ENST00000648423.1:c.112+54del ENSP00000497985.1:n.112+54del
ENST00000648758.1:c.112+54del ENSP00000497731.1:n.112+54del
ENST00000648906.1:n.282+54del
ENST00000649902.1:c.112+54del ENSP00000497216.1:n.112+54del
ENST00000650613.1:n.188+54del
ENST00000374855.8:c.112+54del ENSP00000363988.4:n.112+54del
ENST00000616752.1:c.112+54del ENSP00000481363.1:n.112+54del
NM_000035.3:c.112+54del NP_000026.2:n.112+54del
NM_000035.4:c.112+54del MANE Select NP_000026.2:n.112+54del
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Search 100 bp 3'