Canonical Allele Identifier: CA1127397952

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831165931
• gnomAD v3: 9-101428588-ACT-A
• gnomAD v4: 9-101428588-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428589_101428590del , CM000671.2:g.101428589_101428590del	GRCh38
NC_000009.11:g.104190871_104190872del , CM000671.1:g.104190871_104190872del	GRCh37
NC_000009.10:g.103230692_103230693del	NCBI36
NG_012387.1:g.12191_12192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.325-67_325-66del MANE Select	ENSP00000497767.1:n.325-67_325-66del
ENST00000648064.1:c.325-67_325-66del	ENSP00000497990.1:n.325-67_325-66del
ENST00000648758.1:c.325-67_325-66del	ENSP00000497731.1:n.325-67_325-66del
ENST00000649902.1:c.325-67_325-66del	ENSP00000497216.1:n.325-67_325-66del
ENST00000374855.8:c.325-67_325-66del	ENSP00000363988.4:n.325-67_325-66del
ENST00000468981.3:n.67+1219_67+1220del
ENST00000616752.1:c.325-67_325-66del	ENSP00000481363.1:n.325-67_325-66del
NM_000035.3:c.325-67_325-66del	NP_000026.2:n.325-67_325-66del
NM_000035.4:c.325-67_325-66del MANE Select	NP_000026.2:n.325-67_325-66del