Canonical Allele Identifier: CA374266045

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101429953-G-T
• MyVariant Identifiers: chr9:g.104192235G>T (hg19) ; chr9:g.101429953G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429953G>T , CM000671.2:g.101429953G>T	GRCh38
NC_000009.11:g.104192235G>T , CM000671.1:g.104192235G>T	GRCh37
NC_000009.10:g.103232056G>T	NCBI36
NG_012387.1:g.10828C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.126C>A MANE Select	ENSP00000497767.1:p.Asn42Lys
ENST00000648064.1:c.126C>A	ENSP00000497990.1:p.Asn42Lys
ENST00000648423.1:c.126C>A	ENSP00000497985.1:p.Asn42Lys
ENST00000648758.1:c.126C>A	ENSP00000497731.1:p.Asn42Lys
ENST00000648906.1:n.296C>A
ENST00000649902.1:c.126C>A	ENSP00000497216.1:p.Asn42Lys
ENST00000650613.1:n.202C>A
ENST00000374855.8:c.126C>A	ENSP00000363988.4:p.Asn42Lys
ENST00000616752.1:c.126C>A	ENSP00000481363.1:p.Asn42Lys
NM_000035.3:c.126C>A	NP_000026.2:p.Asn42Lys
NM_000035.4:c.126C>A MANE Select	NP_000026.2:p.Asn42Lys