Canonical Allele Identifier: CA918520752

Gene: ALDOB

Linked Data

• dbSNP Id: rs1588169047

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421905_101421906insATGGCCCGCTTCA , CM000671.2:g.101421905_101421906insATGGCCCGCTTCA	GRCh38
NC_000009.11:g.104184187_104184188insATGGCCCGCTTCA , CM000671.1:g.104184187_104184188insATGGCCCGCTTCA	GRCh37
NC_000009.10:g.103224008_103224009insATGGCCCGCTTCA	NCBI36
NG_012387.1:g.18875_18876insTGAAGCGGGCCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.1000-2_1000-1insTGAAGCGGGCCAT MANE Select	ENSP00000497767.1:n.1000-2_1000-1insTGAAGCGGGCCAT
ENST00000648064.1:c.1000-2_1000-1insTGAAGCGGGCCAT	ENSP00000497990.1:n.1000-2_1000-1insTGAAGCGGGCCAT
ENST00000648758.1:c.1000-2_1000-1insTGAAGCGGGCCAT	ENSP00000497731.1:n.1000-2_1000-1insTGAAGCGGGCCAT
ENST00000374855.8:c.1000-2_1000-1insTGAAGCGGGCCAT	ENSP00000363988.4:n.1000-2_1000-1insTGAAGCGGGCCAT
ENST00000616752.1:c.*12-2_*12-1insTGAAGCGGGCCAT	ENSP00000481363.1:n.*12-2_*12-1insTGAAGCGGGCCAT
NM_000035.3:c.1000-2_1000-1insTGAAGCGGGCCAT	NP_000026.2:n.1000-2_1000-1insTGAAGCGGGCCAT
NM_000035.4:c.1000-2_1000-1insTGAAGCGGGCCAT MANE Select	NP_000026.2:n.1000-2_1000-1insTGAAGCGGGCCAT