Canonical Allele Identifier: CA1868280564
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428590_101428594delinsTAACA , CM000671.2:g.101428590_101428594delinsTAACA GRCh38
NC_000009.11:g.104190872_104190876delinsTAACA , CM000671.1:g.104190872_104190876delinsTAACA GRCh37
NC_000009.10:g.103230693_103230697delinsTAACA NCBI36
NG_012387.1:g.12187_12191delinsTGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-71_325-67delinsTGTTA MANE Select ENSP00000497767.1:n.325-71_325-67delinsTGTTA
ENST00000648064.1:c.325-71_325-67delinsTGTTA ENSP00000497990.1:n.325-71_325-67delinsTGTTA
ENST00000648758.1:c.325-71_325-67delinsTGTTA ENSP00000497731.1:n.325-71_325-67delinsTGTTA
ENST00000649902.1:c.325-71_325-67delinsTGTTA ENSP00000497216.1:n.325-71_325-67delinsTGTTA
ENST00000374855.8:c.325-71_325-67delinsTGTTA ENSP00000363988.4:n.325-71_325-67delinsTGTTA
ENST00000468981.3:n.67+1215_67+1219delinsTGTTA
ENST00000616752.1:c.325-71_325-67delinsTGTTA ENSP00000481363.1:n.325-71_325-67delinsTGTTA
NM_000035.3:c.325-71_325-67delinsTGTTA NP_000026.2:n.325-71_325-67delinsTGTTA
NM_000035.4:c.325-71_325-67delinsTGTTA MANE Select NP_000026.2:n.325-71_325-67delinsTGTTA