Canonical Allele Identifier: CA2691006354

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101429880-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429883_101429884del , CM000671.2:g.101429883_101429884del	GRCh38
NC_000009.11:g.104192165_104192166del , CM000671.1:g.104192165_104192166del	GRCh37
NC_000009.10:g.103231986_103231987del	NCBI36
NG_012387.1:g.10899_10900del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.197_198del MANE Select	ENSP00000497767.1:p.Val66GlyfsTer?
ENST00000648064.1:c.197_198del	ENSP00000497990.1:p.Val66GlyfsTer?
ENST00000648423.1:c.197_198del	ENSP00000497985.1:p.Val66GlyfsTer?
ENST00000648758.1:c.197_198del	ENSP00000497731.1:p.Val66GlyfsTer?
ENST00000648906.1:n.367_368del
ENST00000649902.1:c.197_198del	ENSP00000497216.1:p.Val66GlyfsTer?
ENST00000650613.1:n.273_274del
ENST00000374855.8:c.197_198del	ENSP00000363988.4:p.Val66GlyfsTer?
ENST00000616752.1:c.197_198del	ENSP00000481363.1:p.Val66GlyfsTer?
NM_000035.3:c.197_198del	NP_000026.2:p.Val66GlyfsTer?
NM_000035.4:c.197_198del MANE Select	NP_000026.2:p.Val66GlyfsTer?