Canonical Allele Identifier: CA1868280571
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428616_101428617delinsAG , CM000671.2:g.101428616_101428617delinsAG GRCh38
NC_000009.11:g.104190898_104190899delinsAG , CM000671.1:g.104190898_104190899delinsAG GRCh37
NC_000009.10:g.103230719_103230720delinsAG NCBI36
NG_012387.1:g.12164_12165delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-94_325-93delinsCT MANE Select ENSP00000497767.1:n.325-94_325-93delinsCT
ENST00000648064.1:c.325-94_325-93delinsCT ENSP00000497990.1:n.325-94_325-93delinsCT
ENST00000648758.1:c.325-94_325-93delinsCT ENSP00000497731.1:n.325-94_325-93delinsCT
ENST00000649902.1:c.325-94_325-93delinsCT ENSP00000497216.1:n.325-94_325-93delinsCT
ENST00000374855.8:c.325-94_325-93delinsCT ENSP00000363988.4:n.325-94_325-93delinsCT
ENST00000468981.3:n.67+1192_67+1193delinsCT
ENST00000616752.1:c.325-94_325-93delinsCT ENSP00000481363.1:n.325-94_325-93delinsCT
NM_000035.3:c.325-94_325-93delinsCT NP_000026.2:n.325-94_325-93delinsCT
NM_000035.4:c.325-94_325-93delinsCT MANE Select NP_000026.2:n.325-94_325-93delinsCT