Canonical Allele Identifier: CA2691006255

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101421555-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421558del , CM000671.2:g.101421558del	GRCh38
NC_000009.11:g.104183840del , CM000671.1:g.104183840del	GRCh37
NC_000009.10:g.103223661del	NCBI36
NG_012387.1:g.19225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.*253del MANE Select	ENSP00000497767.1:n.*253del
ENST00000648064.1:c.*253del	ENSP00000497990.1:n.*253del
ENST00000374855.8:c.*253del	ENSP00000363988.4:n.*253del
ENST00000616752.1:c.*360del	ENSP00000481363.1:n.*360del
NM_000035.3:c.*253del	NP_000026.2:n.*253del
NM_000035.4:c.*253del MANE Select	NP_000026.2:n.*253del