Canonical Allele Identifier: CA2691007099

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101425333-C-CTGTGAGATA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425334_101425342dup , CM000671.2:g.101425334_101425342dup	GRCh38
NC_000009.11:g.104187616_104187624dup , CM000671.1:g.104187616_104187624dup	GRCh37
NC_000009.10:g.103227437_103227445dup	NCBI36
NG_012387.1:g.15439_15447dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.799+111_799+119dup MANE Select	ENSP00000497767.1:n.799+111_799+119dup
ENST00000648064.1:c.799+111_799+119dup	ENSP00000497990.1:n.799+111_799+119dup
ENST00000648758.1:c.799+111_799+119dup	ENSP00000497731.1:n.799+111_799+119dup
ENST00000649902.1:c.799+111_799+119dup	ENSP00000497216.1:n.799+111_799+119dup
ENST00000374855.8:c.799+111_799+119dup	ENSP00000363988.4:n.799+111_799+119dup
ENST00000616752.1:c.799+111_799+119dup	ENSP00000481363.1:n.799+111_799+119dup
NM_000035.3:c.799+111_799+119dup	NP_000026.2:n.799+111_799+119dup
NM_000035.4:c.799+111_799+119dup MANE Select	NP_000026.2:n.799+111_799+119dup