Canonical Allele Identifier: CA374265911

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101429888-A-G
• MyVariant Identifiers: chr9:g.104192170A>G (hg19) ; chr9:g.101429888A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429888A>G , CM000671.2:g.101429888A>G	GRCh38
NC_000009.11:g.104192170A>G , CM000671.1:g.104192170A>G	GRCh37
NC_000009.10:g.103231991A>G	NCBI36
NG_012387.1:g.10893T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.191T>C MANE Select	ENSP00000497767.1:p.Phe64Ser
ENST00000648064.1:c.191T>C	ENSP00000497990.1:p.Phe64Ser
ENST00000648423.1:c.191T>C	ENSP00000497985.1:p.Phe64Ser
ENST00000648758.1:c.191T>C	ENSP00000497731.1:p.Phe64Ser
ENST00000648906.1:n.361T>C
ENST00000649902.1:c.191T>C	ENSP00000497216.1:p.Phe64Ser
ENST00000650613.1:n.267T>C
ENST00000374855.8:c.191T>C	ENSP00000363988.4:p.Phe64Ser
ENST00000616752.1:c.191T>C	ENSP00000481363.1:p.Phe64Ser
NM_000035.3:c.191T>C	NP_000026.2:p.Phe64Ser
NM_000035.4:c.191T>C MANE Select	NP_000026.2:p.Phe64Ser