Canonical Allele Identifier: CA2691007755
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428640_101428643del , CM000671.2:g.101428640_101428643del GRCh38
NC_000009.11:g.104190922_104190925del , CM000671.1:g.104190922_104190925del GRCh37
NC_000009.10:g.103230743_103230746del NCBI36
NG_012387.1:g.12139_12142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-119_325-116del MANE Select ENSP00000497767.1:n.325-119_325-116del
ENST00000648064.1:c.325-119_325-116del ENSP00000497990.1:n.325-119_325-116del
ENST00000648758.1:c.325-119_325-116del ENSP00000497731.1:n.325-119_325-116del
ENST00000649902.1:c.325-119_325-116del ENSP00000497216.1:n.325-119_325-116del
ENST00000374855.8:c.325-119_325-116del ENSP00000363988.4:n.325-119_325-116del
ENST00000468981.3:n.67+1167_67+1170del
ENST00000616752.1:c.325-119_325-116del ENSP00000481363.1:n.325-119_325-116del
NM_000035.3:c.325-119_325-116del NP_000026.2:n.325-119_325-116del
NM_000035.4:c.325-119_325-116del MANE Select NP_000026.2:n.325-119_325-116del