Canonical Allele Identifier: CA196957712
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs756749590
gnomAD v2: 9-104190858-ACT-A
gnomAD v3: 9-101428576-ACT-A
gnomAD v4: 9-101428576-ACT-A
MyVariant Identifiers: chr9:g.104190859_104190860del (hg19) chr9:g.101428577_101428578del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428579_101428580del , CM000671.2:g.101428579_101428580del GRCh38
NC_000009.11:g.104190861_104190862del , CM000671.1:g.104190861_104190862del GRCh37
NC_000009.10:g.103230682_103230683del NCBI36
NG_012387.1:g.12203_12204del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-55_325-54del MANE Select ENSP00000497767.1:n.325-55_325-54del
ENST00000648064.1:c.325-55_325-54del ENSP00000497990.1:n.325-55_325-54del
ENST00000648758.1:c.325-55_325-54del ENSP00000497731.1:n.325-55_325-54del
ENST00000649902.1:c.325-55_325-54del ENSP00000497216.1:n.325-55_325-54del
ENST00000374855.8:c.325-55_325-54del ENSP00000363988.4:n.325-55_325-54del
ENST00000468981.3:n.67+1231_67+1232del
ENST00000616752.1:c.325-55_325-54del ENSP00000481363.1:n.325-55_325-54del
NM_000035.3:c.325-55_325-54del NP_000026.2:n.325-55_325-54del
NM_000035.4:c.325-55_325-54del MANE Select NP_000026.2:n.325-55_325-54del
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