Canonical Allele Identifier: CA857733345

Gene: ALDOB

Linked Data

• dbSNP Id: rs1303369795
• gnomAD v3: 9-101427818-TAATA-T
• gnomAD v4: 9-101427818-TAATA-T
• MyVariant Identifiers: chr9:g.104190101_104190104del (hg19) ; chr9:g.101427819_101427822del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427823_101427826del , CM000671.2:g.101427823_101427826del	GRCh38
NC_000009.11:g.104190105_104190108del , CM000671.1:g.104190105_104190108del	GRCh37
NC_000009.10:g.103229926_103229929del	NCBI36
NG_012387.1:g.12959_12962del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.380-180_380-177del MANE Select	ENSP00000497767.1:n.380-180_380-177del
ENST00000648064.1:c.380-180_380-177del	ENSP00000497990.1:n.380-180_380-177del
ENST00000648758.1:c.380-180_380-177del	ENSP00000497731.1:n.380-180_380-177del
ENST00000649902.1:c.380-180_380-177del	ENSP00000497216.1:n.380-180_380-177del
ENST00000374855.8:c.380-180_380-177del	ENSP00000363988.4:n.380-180_380-177del
ENST00000468981.3:n.68-1184_68-1181del
ENST00000616752.1:c.380-180_380-177del	ENSP00000481363.1:n.380-180_380-177del
NM_000035.3:c.380-180_380-177del	NP_000026.2:n.380-180_380-177del
NM_000035.4:c.380-180_380-177del MANE Select	NP_000026.2:n.380-180_380-177del