Canonical Allele Identifier: CA2691005999

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101429698-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429698T>A , CM000671.2:g.101429698T>A	GRCh38
NC_000009.11:g.104191980T>A , CM000671.1:g.104191980T>A	GRCh37
NC_000009.10:g.103231801T>A	NCBI36
NG_012387.1:g.11083A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+57A>T MANE Select	ENSP00000497767.1:n.324+57A>T
ENST00000648064.1:c.324+57A>T	ENSP00000497990.1:n.324+57A>T
ENST00000648758.1:c.324+57A>T	ENSP00000497731.1:n.324+57A>T
ENST00000648906.1:n.551A>T
ENST00000649902.1:c.324+57A>T	ENSP00000497216.1:n.324+57A>T
ENST00000650613.1:n.457A>T
ENST00000374855.8:c.324+57A>T	ENSP00000363988.4:n.324+57A>T
ENST00000468981.3:n.67+111A>T
ENST00000616752.1:c.324+57A>T	ENSP00000481363.1:n.324+57A>T
NM_000035.3:c.324+57A>T	NP_000026.2:n.324+57A>T
NM_000035.4:c.324+57A>T MANE Select	NP_000026.2:n.324+57A>T