Canonical Allele Identifier: CA1127396942

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831119165
• gnomAD v3: 9-101425748-GCTT-G
• gnomAD v4: 9-101425748-GCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425751_101425753del , CM000671.2:g.101425751_101425753del	GRCh38
NC_000009.11:g.104188033_104188035del , CM000671.1:g.104188033_104188035del	GRCh37
NC_000009.10:g.103227854_103227856del	NCBI36
NG_012387.1:g.15030_15032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.625-124_625-122del MANE Select	ENSP00000497767.1:n.625-124_625-122del
ENST00000648064.1:c.625-124_625-122del	ENSP00000497990.1:n.625-124_625-122del
ENST00000648758.1:c.625-124_625-122del	ENSP00000497731.1:n.625-124_625-122del
ENST00000649902.1:c.625-124_625-122del	ENSP00000497216.1:n.625-124_625-122del
ENST00000374855.8:c.625-124_625-122del	ENSP00000363988.4:n.625-124_625-122del
ENST00000468981.3:n.152-124_152-122del
ENST00000616752.1:c.625-124_625-122del	ENSP00000481363.1:n.625-124_625-122del
NM_000035.3:c.625-124_625-122del	NP_000026.2:n.625-124_625-122del
NM_000035.4:c.625-124_625-122del MANE Select	NP_000026.2:n.625-124_625-122del