Canonical Allele Identifier: CA1868275523

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831050403

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421780del , CM000671.2:g.101421780del	GRCh38
NC_000009.11:g.104184062del , CM000671.1:g.104184062del	GRCh37
NC_000009.10:g.103223883del	NCBI36
NG_012387.1:g.19001del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.*29del MANE Select	ENSP00000497767.1:n.*29del
ENST00000648064.1:c.*29del	ENSP00000497990.1:n.*29del
ENST00000648758.1:c.*29del	ENSP00000497731.1:n.*29del
ENST00000374855.8:c.*29del	ENSP00000363988.4:n.*29del
ENST00000616752.1:c.*136del	ENSP00000481363.1:n.*136del
NM_000035.3:c.*29del	NP_000026.2:n.*29del
NM_000035.4:c.*29del MANE Select	NP_000026.2:n.*29del