Canonical Allele Identifier: CA913142081

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104187821dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425539dup , CM000671.2:g.101425539dup	GRCh38
NC_000009.11:g.104187821dup , CM000671.1:g.104187821dup	GRCh37
NC_000009.10:g.103227642dup	NCBI36
NG_012387.1:g.15242dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.713dup MANE Select	ENSP00000497767.1:p.His238GlnfsTer?
ENST00000648064.1:c.713dup	ENSP00000497990.1:p.His238GlnfsTer?
ENST00000648758.1:c.713dup	ENSP00000497731.1:p.His238GlnfsTer?
ENST00000649902.1:c.713dup	ENSP00000497216.1:p.His238GlnfsTer?
ENST00000374855.8:c.713dup	ENSP00000363988.4:p.His238GlnfsTer?
ENST00000616752.1:c.713dup	ENSP00000481363.1:p.His238GlnfsTer?
NM_000035.3:c.713dup	NP_000026.2:p.His238GlnfsTer?
NM_000035.4:c.713dup MANE Select	NP_000026.2:p.His238GlnfsTer?