Canonical Allele Identifier: CA2691007026
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101425175-GAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425177_101425178del , CM000671.2:g.101425177_101425178del GRCh38
NC_000009.11:g.104187459_104187460del , CM000671.1:g.104187459_104187460del GRCh37
NC_000009.10:g.103227280_103227281del NCBI36
NG_012387.1:g.15604_15605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.800-135_800-134del MANE Select ENSP00000497767.1:n.800-135_800-134del
ENST00000648064.1:c.800-135_800-134del ENSP00000497990.1:n.800-135_800-134del
ENST00000648758.1:c.800-135_800-134del ENSP00000497731.1:n.800-135_800-134del
ENST00000649902.1:c.800-135_800-134del ENSP00000497216.1:n.800-135_800-134del
ENST00000374855.8:c.800-135_800-134del ENSP00000363988.4:n.800-135_800-134del
ENST00000616752.1:c.800-135_800-134del ENSP00000481363.1:n.800-135_800-134del
NM_000035.3:c.800-135_800-134del NP_000026.2:n.800-135_800-134del
NM_000035.4:c.800-135_800-134del MANE Select NP_000026.2:n.800-135_800-134del
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