Canonical Allele Identifier: CA374265915

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104192171A>T (hg19) ; chr9:g.101429889A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429889A>T , CM000671.2:g.101429889A>T	GRCh38
NC_000009.11:g.104192171A>T , CM000671.1:g.104192171A>T	GRCh37
NC_000009.10:g.103231992A>T	NCBI36
NG_012387.1:g.10892T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.190T>A MANE Select	ENSP00000497767.1:p.Phe64Ile
ENST00000648064.1:c.190T>A	ENSP00000497990.1:p.Phe64Ile
ENST00000648423.1:c.190T>A	ENSP00000497985.1:p.Phe64Ile
ENST00000648758.1:c.190T>A	ENSP00000497731.1:p.Phe64Ile
ENST00000648906.1:n.360T>A
ENST00000649902.1:c.190T>A	ENSP00000497216.1:p.Phe64Ile
ENST00000650613.1:n.266T>A
ENST00000374855.8:c.190T>A	ENSP00000363988.4:p.Phe64Ile
ENST00000616752.1:c.190T>A	ENSP00000481363.1:p.Phe64Ile
NM_000035.3:c.190T>A	NP_000026.2:p.Phe64Ile
NM_000035.4:c.190T>A MANE Select	NP_000026.2:p.Phe64Ile