Canonical Allele Identifier: CA2691006744

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101424794-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424798del , CM000671.2:g.101424798del	GRCh38
NC_000009.11:g.104187080del , CM000671.1:g.104187080del	GRCh37
NC_000009.10:g.103226901del	NCBI36
NG_012387.1:g.15986del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.999+48del MANE Select	ENSP00000497767.1:n.999+48del
ENST00000648064.1:c.999+48del	ENSP00000497990.1:n.999+48del
ENST00000648758.1:c.999+48del	ENSP00000497731.1:n.999+48del
ENST00000649902.1:c.*18del	ENSP00000497216.1:n.*18del
ENST00000374855.8:c.999+48del	ENSP00000363988.4:n.999+48del
ENST00000616752.1:c.*11+48del	ENSP00000481363.1:n.*11+48del
NM_000035.3:c.999+48del	NP_000026.2:n.999+48del
NM_000035.4:c.999+48del MANE Select	NP_000026.2:n.999+48del