Canonical Allele Identifier: CA2785326720
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428605_101428606insC , CM000671.2:g.101428605_101428606insC GRCh38
NC_000009.11:g.104190887_104190888insC , CM000671.1:g.104190887_104190888insC GRCh37
NC_000009.10:g.103230708_103230709insC NCBI36
NG_012387.1:g.12175_12176insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-83_325-82insG MANE Select ENSP00000497767.1:n.325-83_325-82insG
ENST00000648064.1:c.325-83_325-82insG ENSP00000497990.1:n.325-83_325-82insG
ENST00000648758.1:c.325-83_325-82insG ENSP00000497731.1:n.325-83_325-82insG
ENST00000649902.1:c.325-83_325-82insG ENSP00000497216.1:n.325-83_325-82insG
ENST00000374855.8:c.325-83_325-82insG ENSP00000363988.4:n.325-83_325-82insG
ENST00000468981.3:n.67+1203_67+1204insG
ENST00000616752.1:c.325-83_325-82insG ENSP00000481363.1:n.325-83_325-82insG
NM_000035.3:c.325-83_325-82insG NP_000026.2:n.325-83_325-82insG
NM_000035.4:c.325-83_325-82insG MANE Select NP_000026.2:n.325-83_325-82insG