Canonical Allele Identifier: CA857734480

Gene: ALDOB

Linked Data

• dbSNP Id: rs1464432158
• MyVariant Identifiers: chr9:g.104191763del (hg19) ; chr9:g.101429481del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429483del , CM000671.2:g.101429483del	GRCh38
NC_000009.11:g.104191765del , CM000671.1:g.104191765del	GRCh37
NC_000009.10:g.103231586del	NCBI36
NG_012387.1:g.11300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+274del MANE Select	ENSP00000497767.1:n.324+274del
ENST00000648064.1:c.324+274del	ENSP00000497990.1:n.324+274del
ENST00000648758.1:c.324+274del	ENSP00000497731.1:n.324+274del
ENST00000648906.1:n.768del
ENST00000649902.1:c.324+274del	ENSP00000497216.1:n.324+274del
ENST00000650613.1:n.674del
ENST00000374855.8:c.324+274del	ENSP00000363988.4:n.324+274del
ENST00000468981.3:n.67+328del
ENST00000616752.1:c.324+274del	ENSP00000481363.1:n.324+274del
NM_000035.3:c.324+274del	NP_000026.2:n.324+274del
NM_000035.4:c.324+274del MANE Select	NP_000026.2:n.324+274del