Canonical Allele Identifier: CA1868280607
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428695_101428696delinsAC , CM000671.2:g.101428695_101428696delinsAC GRCh38
NC_000009.11:g.104190977_104190978delinsAC , CM000671.1:g.104190977_104190978delinsAC GRCh37
NC_000009.10:g.103230798_103230799delinsAC NCBI36
NG_012387.1:g.12085_12086delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-173_325-172delinsGT MANE Select ENSP00000497767.1:n.325-173_325-172delinsGT
ENST00000648064.1:c.325-173_325-172delinsGT ENSP00000497990.1:n.325-173_325-172delinsGT
ENST00000648758.1:c.325-173_325-172delinsGT ENSP00000497731.1:n.325-173_325-172delinsGT
ENST00000649902.1:c.325-173_325-172delinsGT ENSP00000497216.1:n.325-173_325-172delinsGT
ENST00000374855.8:c.325-173_325-172delinsGT ENSP00000363988.4:n.325-173_325-172delinsGT
ENST00000468981.3:n.67+1113_67+1114delinsGT
ENST00000616752.1:c.325-173_325-172delinsGT ENSP00000481363.1:n.325-173_325-172delinsGT
NM_000035.3:c.325-173_325-172delinsGT NP_000026.2:n.325-173_325-172delinsGT
NM_000035.4:c.325-173_325-172delinsGT MANE Select NP_000026.2:n.325-173_325-172delinsGT