Canonical Allele Identifier: CA2691006268

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101421571-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421575del , CM000671.2:g.101421575del	GRCh38
NC_000009.11:g.104183857del , CM000671.1:g.104183857del	GRCh37
NC_000009.10:g.103223678del	NCBI36
NG_012387.1:g.19209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.*237del MANE Select	ENSP00000497767.1:n.*237del
ENST00000648064.1:c.*237del	ENSP00000497990.1:n.*237del
ENST00000374855.8:c.*237del	ENSP00000363988.4:n.*237del
ENST00000616752.1:c.*344del	ENSP00000481363.1:n.*344del
NM_000035.3:c.*237del	NP_000026.2:n.*237del
NM_000035.4:c.*237del MANE Select	NP_000026.2:n.*237del