Canonical Allele Identifier: CA2691007152

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101425422-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425424dup , CM000671.2:g.101425424dup	GRCh38
NC_000009.11:g.104187706dup , CM000671.1:g.104187706dup	GRCh37
NC_000009.10:g.103227527dup	NCBI36
NG_012387.1:g.15358dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.799+30dup MANE Select	ENSP00000497767.1:n.799+30dup
ENST00000648064.1:c.799+30dup	ENSP00000497990.1:n.799+30dup
ENST00000648758.1:c.799+30dup	ENSP00000497731.1:n.799+30dup
ENST00000649902.1:c.799+30dup	ENSP00000497216.1:n.799+30dup
ENST00000374855.8:c.799+30dup	ENSP00000363988.4:n.799+30dup
ENST00000616752.1:c.799+30dup	ENSP00000481363.1:n.799+30dup
NM_000035.3:c.799+30dup	NP_000026.2:n.799+30dup
NM_000035.4:c.799+30dup MANE Select	NP_000026.2:n.799+30dup