Canonical Allele Identifier: CA1868280507

Gene: ALDOB

Linked Data

• dbSNP Id: rs387906225

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428491_101428494dup , CM000671.2:g.101428491_101428494dup	GRCh38
NC_000009.11:g.104190773_104190776dup , CM000671.1:g.104190773_104190776dup	GRCh37
NC_000009.10:g.103230594_103230597dup	NCBI36
NG_012387.1:g.12293_12296dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.360_363dup MANE Select	ENSP00000497767.1:p.Glu122GlnfsTer9
ENST00000648064.1:c.360_363dup	ENSP00000497990.1:p.Glu122GlnfsTer9
ENST00000648758.1:c.360_363dup	ENSP00000497731.1:p.Glu122GlnfsTer9
ENST00000649902.1:c.360_363dup	ENSP00000497216.1:p.Glu122GlnfsTer9
ENST00000374855.8:c.360_363dup	ENSP00000363988.4:p.Glu122GlnfsTer9
ENST00000468981.3:n.67+1321_67+1324dup
ENST00000616752.1:c.360_363dup	ENSP00000481363.1:p.Glu122GlnfsTer9
NM_000035.3:c.360_363dup	NP_000026.2:p.Glu122GlnfsTer9
NM_000035.4:c.360_363dup MANE Select	NP_000026.2:p.Glu122GlnfsTer9