Canonical Allele Identifier: CA2691007162
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425561del , CM000671.2:g.101425561del GRCh38
NC_000009.11:g.104187843del , CM000671.1:g.104187843del GRCh37
NC_000009.10:g.103227664del NCBI36
NG_012387.1:g.15222del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.693del MANE Select ENSP00000497767.1:p.Asn232ThrfsTer3
ENST00000648064.1:c.693del ENSP00000497990.1:p.Asn232ThrfsTer3
ENST00000648758.1:c.693del ENSP00000497731.1:p.Asn232ThrfsTer3
ENST00000649902.1:c.693del ENSP00000497216.1:p.Asn232ThrfsTer3
ENST00000374855.8:c.693del ENSP00000363988.4:p.Asn232ThrfsTer3
ENST00000616752.1:c.693del ENSP00000481363.1:p.Asn232ThrfsTer3
NM_000035.3:c.693del NP_000026.2:p.Asn232ThrfsTer3
NM_000035.4:c.693del MANE Select NP_000026.2:p.Asn232ThrfsTer3