Canonical Allele Identifier: CA857731459

Gene: ALDOB

Linked Data

• dbSNP Id: rs1288599712
• gnomAD v3: 9-101425699-C-CA
• gnomAD v4: 9-101425699-C-CA
• MyVariant Identifiers: chr9:g.104187981_104187982insA (hg19) ; chr9:g.101425699_101425700insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425700dup , CM000671.2:g.101425700dup	GRCh38
NC_000009.11:g.104187982dup , CM000671.1:g.104187982dup	GRCh37
NC_000009.10:g.103227803dup	NCBI36
NG_012387.1:g.15081dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.625-73dup MANE Select	ENSP00000497767.1:n.625-73dup
ENST00000648064.1:c.625-73dup	ENSP00000497990.1:n.625-73dup
ENST00000648758.1:c.625-73dup	ENSP00000497731.1:n.625-73dup
ENST00000649902.1:c.625-73dup	ENSP00000497216.1:n.625-73dup
ENST00000374855.8:c.625-73dup	ENSP00000363988.4:n.625-73dup
ENST00000468981.3:n.152-73dup
ENST00000616752.1:c.625-73dup	ENSP00000481363.1:n.625-73dup
NM_000035.3:c.625-73dup	NP_000026.2:n.625-73dup
NM_000035.4:c.625-73dup MANE Select	NP_000026.2:n.625-73dup