Canonical Allele Identifier: CA196956706

Gene: ALDOB

Linked Data

• dbSNP Id: rs567021455
• gnomAD v2: 9-104187596-GAGA-G
• gnomAD v3: 9-101425314-GAGA-G
• gnomAD v4: 9-101425314-GAGA-G
• MyVariant Identifiers: chr9:g.104187597_104187599del (hg19) ; chr9:g.101425315_101425317del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425320_101425322del , CM000671.2:g.101425320_101425322del	GRCh38
NC_000009.11:g.104187602_104187604del , CM000671.1:g.104187602_104187604del	GRCh37
NC_000009.10:g.103227423_103227425del	NCBI36
NG_012387.1:g.15464_15466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.799+136_799+138del MANE Select	ENSP00000497767.1:n.799+136_799+138del
ENST00000648064.1:c.799+136_799+138del	ENSP00000497990.1:n.799+136_799+138del
ENST00000648758.1:c.799+136_799+138del	ENSP00000497731.1:n.799+136_799+138del
ENST00000649902.1:c.799+136_799+138del	ENSP00000497216.1:n.799+136_799+138del
ENST00000374855.8:c.799+136_799+138del	ENSP00000363988.4:n.799+136_799+138del
ENST00000616752.1:c.799+136_799+138del	ENSP00000481363.1:n.799+136_799+138del
NM_000035.3:c.799+136_799+138del	NP_000026.2:n.799+136_799+138del
NM_000035.4:c.799+136_799+138del MANE Select	NP_000026.2:n.799+136_799+138del