Canonical Allele Identifier: CA466463003

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104192067G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429785G>T , CM000671.2:g.101429785G>T	GRCh38
NC_000009.11:g.104192067G>T , CM000671.1:g.104192067G>T	GRCh37
NC_000009.10:g.103231888G>T	NCBI36
NG_012387.1:g.10996C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.294C>A MANE Select	ENSP00000497767.1:p.Leu98=
ENST00000648064.1:c.294C>A	ENSP00000497990.1:p.Leu98=
ENST00000648758.1:c.294C>A	ENSP00000497731.1:p.Leu98=
ENST00000648906.1:n.464C>A
ENST00000649902.1:c.294C>A	ENSP00000497216.1:p.Leu98=
ENST00000650613.1:n.370C>A
ENST00000374855.8:c.294C>A	ENSP00000363988.4:p.Leu98=
ENST00000468981.3:n.67+24C>A
ENST00000616752.1:c.294C>A	ENSP00000481363.1:p.Leu98=
NM_000035.3:c.294C>A	NP_000026.2:p.Leu98=
NM_000035.4:c.294C>A MANE Select	NP_000026.2:p.Leu98=