Canonical Allele Identifier: CA1868278326
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831097441

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424768_101424770del , CM000671.2:g.101424768_101424770del GRCh38
NC_000009.11:g.104187050_104187052del , CM000671.1:g.104187050_104187052del GRCh37
NC_000009.10:g.103226871_103226873del NCBI36
NG_012387.1:g.16011_16013del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.999+73_999+75del MANE Select ENSP00000497767.1:n.999+73_999+75del
ENST00000648064.1:c.999+73_999+75del ENSP00000497990.1:n.999+73_999+75del
ENST00000648758.1:c.999+73_999+75del ENSP00000497731.1:n.999+73_999+75del
ENST00000649902.1:c.*43_*45del ENSP00000497216.1:n.*43_*45del
ENST00000374855.8:c.999+73_999+75del ENSP00000363988.4:n.999+73_999+75del
ENST00000616752.1:c.*11+73_*11+75del ENSP00000481363.1:n.*11+73_*11+75del
NM_000035.3:c.999+73_999+75del NP_000026.2:n.999+73_999+75del
NM_000035.4:c.999+73_999+75del MANE Select NP_000026.2:n.999+73_999+75del