Canonical Allele Identifier: CA5161675

Gene: ALDOB

Linked Data

• dbSNP Id: rs772903939
• ExAC: 9:104192033 TCACCTTGATTCC / T
• gnomAD v2: 9-104192033-TCACCTTGATTCC-T
• MyVariant Identifiers: chr9:g.104192034_104192045del (hg19) ; chr9:g.101429752_101429763del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429756_101429767del , CM000671.2:g.101429756_101429767del	GRCh38
NC_000009.11:g.104192038_104192049del , CM000671.1:g.104192038_104192049del	GRCh37
NC_000009.10:g.103231859_103231870del	NCBI36
NG_012387.1:g.11018_11029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.316_324+3del
ENST00000648064.1:c.316_324+3del
ENST00000648758.1:c.316_324+3del
ENST00000648906.1:n.486_497del
ENST00000649902.1:c.316_324+3del
ENST00000650613.1:n.392_403del
ENST00000374855.8:c.316_324+3del
ENST00000468981.3:n.67+46_67+57del
ENST00000616752.1:c.316_324+3del
NM_000035.3:c.316_324+3del
NM_000035.4:c.316_324+3del