Canonical Allele Identifier: CA1127398845
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831196439
gnomAD v3: 9-101430117-CA-C
gnomAD v4: 9-101430117-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101430118del , CM000671.2:g.101430118del GRCh38
NC_000009.11:g.104192400del , CM000671.1:g.104192400del GRCh37
NC_000009.10:g.103232221del NCBI36
NG_012387.1:g.10663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.113-152del MANE Select ENSP00000497767.1:n.113-152del
ENST00000648064.1:c.113-152del ENSP00000497990.1:n.113-152del
ENST00000648423.1:c.113-152del ENSP00000497985.1:n.113-152del
ENST00000648758.1:c.113-152del ENSP00000497731.1:n.113-152del
ENST00000648906.1:n.283-152del
ENST00000649902.1:c.113-152del ENSP00000497216.1:n.113-152del
ENST00000650613.1:n.189-152del
ENST00000374855.8:c.113-152del ENSP00000363988.4:n.113-152del
ENST00000616752.1:c.113-152del ENSP00000481363.1:n.113-152del
NM_000035.3:c.113-152del NP_000026.2:n.113-152del
NM_000035.4:c.113-152del MANE Select NP_000026.2:n.113-152del
Search 100 bp 5'
Search 100 bp 3'