Canonical Allele Identifier: CA2691007726

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101428586-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428586_101428587insC , CM000671.2:g.101428586_101428587insC	GRCh38
NC_000009.11:g.104190868_104190869insC , CM000671.1:g.104190868_104190869insC	GRCh37
NC_000009.10:g.103230689_103230690insC	NCBI36
NG_012387.1:g.12194_12195insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.325-64_325-63insG MANE Select	ENSP00000497767.1:n.325-64_325-63insG
ENST00000648064.1:c.325-64_325-63insG	ENSP00000497990.1:n.325-64_325-63insG
ENST00000648758.1:c.325-64_325-63insG	ENSP00000497731.1:n.325-64_325-63insG
ENST00000649902.1:c.325-64_325-63insG	ENSP00000497216.1:n.325-64_325-63insG
ENST00000374855.8:c.325-64_325-63insG	ENSP00000363988.4:n.325-64_325-63insG
ENST00000468981.3:n.67+1222_67+1223insG
ENST00000616752.1:c.325-64_325-63insG	ENSP00000481363.1:n.325-64_325-63insG
NM_000035.3:c.325-64_325-63insG	NP_000026.2:n.325-64_325-63insG
NM_000035.4:c.325-64_325-63insG MANE Select	NP_000026.2:n.325-64_325-63insG