Canonical Allele Identifier: CA2579403693

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101427419-AAAGAAAAGCTCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427427_101427439del , CM000671.2:g.101427427_101427439del	GRCh38
NC_000009.11:g.104189709_104189721del , CM000671.1:g.104189709_104189721del	GRCh37
NC_000009.10:g.103229530_103229542del	NCBI36
NG_012387.1:g.13349_13361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.540+50_540+62del MANE Select	ENSP00000497767.1:n.540+50_540+62del
ENST00000648064.1:c.540+50_540+62del	ENSP00000497990.1:n.540+50_540+62del
ENST00000648758.1:c.540+50_540+62del	ENSP00000497731.1:n.540+50_540+62del
ENST00000649902.1:c.540+50_540+62del	ENSP00000497216.1:n.540+50_540+62del
ENST00000374855.8:c.540+50_540+62del	ENSP00000363988.4:n.540+50_540+62del
ENST00000468981.3:n.68-794_68-782del
ENST00000616752.1:c.540+50_540+62del	ENSP00000481363.1:n.540+50_540+62del
NM_000035.3:c.540+50_540+62del	NP_000026.2:n.540+50_540+62del
NM_000035.4:c.540+50_540+62del MANE Select	NP_000026.2:n.540+50_540+62del