Canonical Allele Identifier: CA918520502

Gene: ALDOB

Linked Data

• dbSNP Id: rs1588171805

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428777_101428782del , CM000671.2:g.101428777_101428782del	GRCh38
NC_000009.11:g.104191059_104191064del , CM000671.1:g.104191059_104191064del	GRCh37
NC_000009.10:g.103230880_103230885del	NCBI36
NG_012387.1:g.12001_12006del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.325-257_325-252del MANE Select	ENSP00000497767.1:n.325-257_325-252del
ENST00000648064.1:c.325-257_325-252del	ENSP00000497990.1:n.325-257_325-252del
ENST00000648758.1:c.325-257_325-252del	ENSP00000497731.1:n.325-257_325-252del
ENST00000649902.1:c.325-257_325-252del	ENSP00000497216.1:n.325-257_325-252del
ENST00000374855.8:c.325-257_325-252del	ENSP00000363988.4:n.325-257_325-252del
ENST00000468981.3:n.67+1029_67+1034del
ENST00000616752.1:c.325-257_325-252del	ENSP00000481363.1:n.325-257_325-252del
NM_000035.3:c.325-257_325-252del	NP_000026.2:n.325-257_325-252del
NM_000035.4:c.325-257_325-252del MANE Select	NP_000026.2:n.325-257_325-252del