Canonical Allele Identifier: CA857732898

Gene: ALDOB

Linked Data

• dbSNP Id: rs1196113741
• gnomAD v3: 9-101427452-C-CT
• gnomAD v4: 9-101427452-C-CT
• MyVariant Identifiers: chr9:g.104189734_104189735insT (hg19) ; chr9:g.101427452_101427453insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427457dup , CM000671.2:g.101427457dup	GRCh38
NC_000009.11:g.104189739dup , CM000671.1:g.104189739dup	GRCh37
NC_000009.10:g.103229560dup	NCBI36
NG_012387.1:g.13328dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.540+29dup MANE Select	ENSP00000497767.1:n.540+29dup
ENST00000648064.1:c.540+29dup	ENSP00000497990.1:n.540+29dup
ENST00000648758.1:c.540+29dup	ENSP00000497731.1:n.540+29dup
ENST00000649902.1:c.540+29dup	ENSP00000497216.1:n.540+29dup
ENST00000374855.8:c.540+29dup	ENSP00000363988.4:n.540+29dup
ENST00000468981.3:n.68-815dup
ENST00000616752.1:c.540+29dup	ENSP00000481363.1:n.540+29dup
NM_000035.3:c.540+29dup	NP_000026.2:n.540+29dup
NM_000035.4:c.540+29dup MANE Select	NP_000026.2:n.540+29dup