Canonical Allele Identifier: CA2785326718

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428569_101428570insCCAAACACACCC , CM000671.2:g.101428569_101428570insCCAAACACACCC	GRCh38
NC_000009.11:g.104190851_104190852insCCAAACACACCC , CM000671.1:g.104190851_104190852insCCAAACACACCC	GRCh37
NC_000009.10:g.103230672_103230673insCCAAACACACCC	NCBI36
NG_012387.1:g.12211_12212insGGGTGTGTTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.325-47_325-46insGGGTGTGTTTGG MANE Select	ENSP00000497767.1:n.325-47_325-46insGGGTGTGTTTGG
ENST00000648064.1:c.325-47_325-46insGGGTGTGTTTGG	ENSP00000497990.1:n.325-47_325-46insGGGTGTGTTTGG
ENST00000648758.1:c.325-47_325-46insGGGTGTGTTTGG	ENSP00000497731.1:n.325-47_325-46insGGGTGTGTTTGG
ENST00000649902.1:c.325-47_325-46insGGGTGTGTTTGG	ENSP00000497216.1:n.325-47_325-46insGGGTGTGTTTGG
ENST00000374855.8:c.325-47_325-46insGGGTGTGTTTGG	ENSP00000363988.4:n.325-47_325-46insGGGTGTGTTTGG
ENST00000468981.3:n.67+1239_67+1240insGGGTGTGTTTGG
ENST00000616752.1:c.325-47_325-46insGGGTGTGTTTGG	ENSP00000481363.1:n.325-47_325-46insGGGTGTGTTTGG
NM_000035.3:c.325-47_325-46insGGGTGTGTTTGG	NP_000026.2:n.325-47_325-46insGGGTGTGTTTGG
NM_000035.4:c.325-47_325-46insGGGTGTGTTTGG MANE Select	NP_000026.2:n.325-47_325-46insGGGTGTGTTTGG