Canonical Allele Identifier: CA857732909
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1261554319
MyVariant Identifiers: chr9:g.104189747_104189748insG (hg19) chr9:g.101427465_101427466insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427469dup , CM000671.2:g.101427469dup GRCh38
NC_000009.11:g.104189751dup , CM000671.1:g.104189751dup GRCh37
NC_000009.10:g.103229572dup NCBI36
NG_012387.1:g.13315dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.540+16dup MANE Select ENSP00000497767.1:n.540+16dup
ENST00000648064.1:c.540+16dup ENSP00000497990.1:n.540+16dup
ENST00000648758.1:c.540+16dup ENSP00000497731.1:n.540+16dup
ENST00000649902.1:c.540+16dup ENSP00000497216.1:n.540+16dup
ENST00000374855.8:c.540+16dup ENSP00000363988.4:n.540+16dup
ENST00000468981.3:n.68-828dup
ENST00000616752.1:c.540+16dup ENSP00000481363.1:n.540+16dup
NM_000035.3:c.540+16dup NP_000026.2:n.540+16dup
NM_000035.4:c.540+16dup MANE Select NP_000026.2:n.540+16dup
Search 100 bp 5'
Search 100 bp 3'