Canonical Allele Identifier: CA857734578
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1294040800
gnomAD v3: 9-101429661-AG-A
gnomAD v4: 9-101429661-AG-A
MyVariant Identifiers: chr9:g.104191944del (hg19) chr9:g.101429662del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429663del , CM000671.2:g.101429663del GRCh38
NC_000009.11:g.104191945del , CM000671.1:g.104191945del GRCh37
NC_000009.10:g.103231766del NCBI36
NG_012387.1:g.11119del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.324+93del MANE Select ENSP00000497767.1:n.324+93del
ENST00000648064.1:c.324+93del ENSP00000497990.1:n.324+93del
ENST00000648758.1:c.324+93del ENSP00000497731.1:n.324+93del
ENST00000648906.1:n.587del
ENST00000649902.1:c.324+93del ENSP00000497216.1:n.324+93del
ENST00000650613.1:n.493del
ENST00000374855.8:c.324+93del ENSP00000363988.4:n.324+93del
ENST00000468981.3:n.67+147del
ENST00000616752.1:c.324+93del ENSP00000481363.1:n.324+93del
NM_000035.3:c.324+93del NP_000026.2:n.324+93del
NM_000035.4:c.324+93del MANE Select NP_000026.2:n.324+93del
Search 100 bp 5'
Search 100 bp 3'