Canonical Allele Identifier: CA2691005966

Gene: ALDOB

Linked Data

• dbSNP Id: rs2118361691
• gnomAD v4: 9-101429672-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429675_101429676del , CM000671.2:g.101429675_101429676del	GRCh38
NC_000009.11:g.104191957_104191958del , CM000671.1:g.104191957_104191958del	GRCh37
NC_000009.10:g.103231778_103231779del	NCBI36
NG_012387.1:g.11107_11108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+81_324+82del MANE Select	ENSP00000497767.1:n.324+81_324+82del
ENST00000648064.1:c.324+81_324+82del	ENSP00000497990.1:n.324+81_324+82del
ENST00000648758.1:c.324+81_324+82del	ENSP00000497731.1:n.324+81_324+82del
ENST00000648906.1:n.575_576del
ENST00000649902.1:c.324+81_324+82del	ENSP00000497216.1:n.324+81_324+82del
ENST00000650613.1:n.481_482del
ENST00000374855.8:c.324+81_324+82del	ENSP00000363988.4:n.324+81_324+82del
ENST00000468981.3:n.67+135_67+136del
ENST00000616752.1:c.324+81_324+82del	ENSP00000481363.1:n.324+81_324+82del
NM_000035.3:c.324+81_324+82del	NP_000026.2:n.324+81_324+82del
NM_000035.4:c.324+81_324+82del MANE Select	NP_000026.2:n.324+81_324+82del