Canonical Allele Identifier: CA1868278356

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831098096

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424813_101424815del , CM000671.2:g.101424813_101424815del	GRCh38
NC_000009.11:g.104187095_104187097del , CM000671.1:g.104187095_104187097del	GRCh37
NC_000009.10:g.103226916_103226918del	NCBI36
NG_012387.1:g.15971_15973del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.999+33_999+35del MANE Select	ENSP00000497767.1:n.999+33_999+35del
ENST00000648064.1:c.999+33_999+35del	ENSP00000497990.1:n.999+33_999+35del
ENST00000648758.1:c.999+33_999+35del	ENSP00000497731.1:n.999+33_999+35del
ENST00000649902.1:c.*3_*5del	ENSP00000497216.1:n.*3_*5del
ENST00000374855.8:c.999+33_999+35del	ENSP00000363988.4:n.999+33_999+35del
ENST00000616752.1:c.*11+33_*11+35del	ENSP00000481363.1:n.*11+33_*11+35del
NM_000035.3:c.999+33_999+35del	NP_000026.2:n.999+33_999+35del
NM_000035.4:c.999+33_999+35del MANE Select	NP_000026.2:n.999+33_999+35del