Canonical Allele Identifier: CA2691006359

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101429884-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429885del , CM000671.2:g.101429885del	GRCh38
NC_000009.11:g.104192167del , CM000671.1:g.104192167del	GRCh37
NC_000009.10:g.103231988del	NCBI36
NG_012387.1:g.10896del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.194del MANE Select	ENSP00000497767.1:p.Ser65LeufsTer13
ENST00000648064.1:c.194del	ENSP00000497990.1:p.Ser65LeufsTer13
ENST00000648423.1:c.194del	ENSP00000497985.1:p.Ser65LeufsTer?
ENST00000648758.1:c.194del	ENSP00000497731.1:p.Ser65LeufsTer13
ENST00000648906.1:n.364del
ENST00000649902.1:c.194del	ENSP00000497216.1:p.Ser65LeufsTer13
ENST00000650613.1:n.270del
ENST00000374855.8:c.194del	ENSP00000363988.4:p.Ser65LeufsTer13
ENST00000616752.1:c.194del	ENSP00000481363.1:p.Ser65LeufsTer13
NM_000035.3:c.194del	NP_000026.2:p.Ser65LeufsTer13
NM_000035.4:c.194del MANE Select	NP_000026.2:p.Ser65LeufsTer13