Canonical Allele Identifier: CA114312
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101426628_101426633del , CM000671.2:g.101426628_101426633del GRCh38
NC_000009.11:g.104188910_104188915del , CM000671.1:g.104188910_104188915del GRCh37
NC_000009.10:g.103228731_103228736del NCBI36
NG_012387.1:g.14150_14155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.548_553del MANE Select ENSP00000497767.1:p.Leu183_Val184del
ENST00000648064.1:c.548_553del ENSP00000497990.1:p.Leu183_Val184del
ENST00000648758.1:c.548_553del ENSP00000497731.1:p.Leu183_Val184del
ENST00000649902.1:c.548_553del ENSP00000497216.1:p.Leu183_Val184del
ENST00000374855.8:c.548_553del ENSP00000363988.4:p.Leu183_Val184del
ENST00000468981.3:n.75_80del
ENST00000616752.1:c.548_553del ENSP00000481363.1:p.Leu183_Val184del
NM_000035.3:c.548_553del NP_000026.2:p.Leu183_Val184del
NM_000035.4:c.548_553del MANE Select NP_000026.2:p.Leu183_Val184del