Canonical Allele Identifier: CA857730889

Gene: ALDOB

Linked Data

• dbSNP Id: rs1450927976
• gnomAD v3: 9-101425281-GGCA-G
• gnomAD v4: 9-101425281-GGCA-G
• MyVariant Identifiers: chr9:g.104187564_104187566del (hg19) ; chr9:g.101425282_101425284del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425283_101425285del , CM000671.2:g.101425283_101425285del	GRCh38
NC_000009.11:g.104187565_104187567del , CM000671.1:g.104187565_104187567del	GRCh37
NC_000009.10:g.103227386_103227388del	NCBI36
NG_012387.1:g.15497_15499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.799+169_799+171del MANE Select	ENSP00000497767.1:n.799+169_799+171del
ENST00000648064.1:c.799+169_799+171del	ENSP00000497990.1:n.799+169_799+171del
ENST00000648758.1:c.799+169_799+171del	ENSP00000497731.1:n.799+169_799+171del
ENST00000649902.1:c.799+169_799+171del	ENSP00000497216.1:n.799+169_799+171del
ENST00000374855.8:c.799+169_799+171del	ENSP00000363988.4:n.799+169_799+171del
ENST00000616752.1:c.799+169_799+171del	ENSP00000481363.1:n.799+169_799+171del
NM_000035.3:c.799+169_799+171del	NP_000026.2:n.799+169_799+171del
NM_000035.4:c.799+169_799+171del MANE Select	NP_000026.2:n.799+169_799+171del