Canonical Allele Identifier: CA2720258730
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs2118345224

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425456del , CM000671.2:g.101425456del GRCh38
NC_000009.11:g.104187738del , CM000671.1:g.104187738del GRCh37
NC_000009.10:g.103227559del NCBI36
NG_012387.1:g.15326del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.797del MANE Select ENSP00000497767.1:p.Pro266LeufsTer10
ENST00000648064.1:c.797del ENSP00000497990.1:p.Pro266LeufsTer10
ENST00000648758.1:c.797del ENSP00000497731.1:p.Pro266LeufsTer10
ENST00000649902.1:c.797del ENSP00000497216.1:p.Pro266LeufsTer10
ENST00000374855.8:c.797del ENSP00000363988.4:p.Pro266LeufsTer10
ENST00000616752.1:c.797del ENSP00000481363.1:p.Pro266LeufsTer10
NM_000035.3:c.797del NP_000026.2:p.Pro266LeufsTer10
NM_000035.4:c.797del MANE Select NP_000026.2:p.Pro266LeufsTer10