Canonical Allele Identifier: CA196957931

Gene: ALDOB

Linked Data

• dbSNP Id: rs960556442
• gnomAD v3: 9-101429469-T-TA
• gnomAD v4: 9-101429469-T-TA
• MyVariant Identifiers: chr9:g.104191751_104191752insA (hg19) ; chr9:g.101429469_101429470insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429470dup , CM000671.2:g.101429470dup	GRCh38
NC_000009.11:g.104191752dup , CM000671.1:g.104191752dup	GRCh37
NC_000009.10:g.103231573dup	NCBI36
NG_012387.1:g.11311dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+285dup MANE Select	ENSP00000497767.1:n.324+285dup
ENST00000648064.1:c.324+285dup	ENSP00000497990.1:n.324+285dup
ENST00000648758.1:c.324+285dup	ENSP00000497731.1:n.324+285dup
ENST00000648906.1:n.779dup
ENST00000649902.1:c.324+285dup	ENSP00000497216.1:n.324+285dup
ENST00000650613.1:n.685dup
ENST00000374855.8:c.324+285dup	ENSP00000363988.4:n.324+285dup
ENST00000468981.3:n.67+339dup
ENST00000616752.1:c.324+285dup	ENSP00000481363.1:n.324+285dup
NM_000035.3:c.324+285dup	NP_000026.2:n.324+285dup
NM_000035.4:c.324+285dup MANE Select	NP_000026.2:n.324+285dup