Canonical Allele Identifier: CA374265782

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104192108A>C (hg19) ; chr9:g.101429826A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429826A>C , CM000671.2:g.101429826A>C	GRCh38
NC_000009.11:g.104192108A>C , CM000671.1:g.104192108A>C	GRCh37
NC_000009.10:g.103231929A>C	NCBI36
NG_012387.1:g.10955T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.253T>G MANE Select	ENSP00000497767.1:p.Tyr85Asp
ENST00000648064.1:c.253T>G	ENSP00000497990.1:p.Tyr85Asp
ENST00000648758.1:c.253T>G	ENSP00000497731.1:p.Tyr85Asp
ENST00000648906.1:n.423T>G
ENST00000649902.1:c.253T>G	ENSP00000497216.1:p.Tyr85Asp
ENST00000650613.1:n.329T>G
ENST00000374855.8:c.253T>G	ENSP00000363988.4:p.Tyr85Asp
ENST00000468981.3:n.50T>G
ENST00000616752.1:c.253T>G	ENSP00000481363.1:p.Tyr85Asp
NM_000035.3:c.253T>G	NP_000026.2:p.Tyr85Asp
NM_000035.4:c.253T>G MANE Select	NP_000026.2:p.Tyr85Asp