Canonical Allele Identifier: CA1868275521
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421779_101421780delinsCA , CM000671.2:g.101421779_101421780delinsCA GRCh38
NC_000009.11:g.104184061_104184062delinsCA , CM000671.1:g.104184061_104184062delinsCA GRCh37
NC_000009.10:g.103223882_103223883delinsCA NCBI36
NG_012387.1:g.19001_19002delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*29_*30delinsTG MANE Select ENSP00000497767.1:n.*29_*30delinsTG
ENST00000648064.1:c.*29_*30delinsTG ENSP00000497990.1:n.*29_*30delinsTG
ENST00000648758.1:c.*29_*30delinsTG ENSP00000497731.1:n.*29_*30delinsTG
ENST00000374855.8:c.*29_*30delinsTG ENSP00000363988.4:n.*29_*30delinsTG
ENST00000616752.1:c.*136_*137delinsTG ENSP00000481363.1:n.*136_*137delinsTG
NM_000035.3:c.*29_*30delinsTG NP_000026.2:n.*29_*30delinsTG
NM_000035.4:c.*29_*30delinsTG MANE Select NP_000026.2:n.*29_*30delinsTG