Canonical Allele Identifier: CA2691007156
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425443_101425445dup , CM000671.2:g.101425443_101425445dup GRCh38
NC_000009.11:g.104187725_104187727dup , CM000671.1:g.104187725_104187727dup GRCh37
NC_000009.10:g.103227546_103227548dup NCBI36
NG_012387.1:g.15339_15341dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.799+11_799+13dup MANE Select ENSP00000497767.1:n.799+11_799+13dup
ENST00000648064.1:c.799+11_799+13dup ENSP00000497990.1:n.799+11_799+13dup
ENST00000648758.1:c.799+11_799+13dup ENSP00000497731.1:n.799+11_799+13dup
ENST00000649902.1:c.799+11_799+13dup ENSP00000497216.1:n.799+11_799+13dup
ENST00000374855.8:c.799+11_799+13dup ENSP00000363988.4:n.799+11_799+13dup
ENST00000616752.1:c.799+11_799+13dup ENSP00000481363.1:n.799+11_799+13dup
NM_000035.3:c.799+11_799+13dup NP_000026.2:n.799+11_799+13dup
NM_000035.4:c.799+11_799+13dup MANE Select NP_000026.2:n.799+11_799+13dup