Canonical Allele Identifier: CA1127398830

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831195676
• gnomAD v3: 9-101430069-CTT-C
• gnomAD v4: 9-101430069-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430071_101430072del , CM000671.2:g.101430071_101430072del	GRCh38
NC_000009.11:g.104192353_104192354del , CM000671.1:g.104192353_104192354del	GRCh37
NC_000009.10:g.103232174_103232175del	NCBI36
NG_012387.1:g.10710_10711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.113-105_113-104del MANE Select	ENSP00000497767.1:n.113-105_113-104del
ENST00000648064.1:c.113-105_113-104del	ENSP00000497990.1:n.113-105_113-104del
ENST00000648423.1:c.113-105_113-104del	ENSP00000497985.1:n.113-105_113-104del
ENST00000648758.1:c.113-105_113-104del	ENSP00000497731.1:n.113-105_113-104del
ENST00000648906.1:n.283-105_283-104del
ENST00000649902.1:c.113-105_113-104del	ENSP00000497216.1:n.113-105_113-104del
ENST00000650613.1:n.189-105_189-104del
ENST00000374855.8:c.113-105_113-104del	ENSP00000363988.4:n.113-105_113-104del
ENST00000616752.1:c.113-105_113-104del	ENSP00000481363.1:n.113-105_113-104del
NM_000035.3:c.113-105_113-104del	NP_000026.2:n.113-105_113-104del
NM_000035.4:c.113-105_113-104del MANE Select	NP_000026.2:n.113-105_113-104del