Canonical Allele Identifier: CA1868278863
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831108057
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425231del , CM000671.2:g.101425231del GRCh38
NC_000009.11:g.104187513del , CM000671.1:g.104187513del GRCh37
NC_000009.10:g.103227334del NCBI36
NG_012387.1:g.15550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.800-189del MANE Select ENSP00000497767.1:n.800-189del
ENST00000648064.1:c.800-189del ENSP00000497990.1:n.800-189del
ENST00000648758.1:c.800-189del ENSP00000497731.1:n.800-189del
ENST00000649902.1:c.800-189del ENSP00000497216.1:n.800-189del
ENST00000374855.8:c.800-189del ENSP00000363988.4:n.800-189del
ENST00000616752.1:c.800-189del ENSP00000481363.1:n.800-189del
NM_000035.3:c.800-189del NP_000026.2:n.800-189del
NM_000035.4:c.800-189del MANE Select NP_000026.2:n.800-189del
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Search 100 bp 3'