Canonical Allele Identifier: CA2785321923

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424882_101424883insACGGACGAGGCTGGGGTGGCCTTCGTCTGTCACGAGGAGGCGACGGATTCGCTCGGGGC , CM000671.2:g.101424882_101424883insACGGACGAGGCTGGGGTGGCCTTCGTCTGTCACGAGGAGGCGACGGATTCGCTCGGGGC	GRCh38
NC_000009.11:g.104187164_104187165insACGGACGAGGCTGGGGTGGCCTTCGTCTGTCACGAGGAGGCGACGGATTCGCTCGGGGC , CM000671.1:g.104187164_104187165insACGGACGAGGCTGGGGTGGCCTTCGTCTGTCACGAGGAGGCGACGGATTCGCTCGGGGC	GRCh37
NC_000009.10:g.103226985_103226986insACGGACGAGGCTGGGGTGGCCTTCGTCTGTCACGAGGAGGCGACGGATTCGCTCGGGGC	NCBI36
NG_012387.1:g.15898_15899insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT MANE Select	ENSP00000497767.1:p.Asn320LysfsTer30
ENST00000648064.1:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT	ENSP00000497990.1:p.Asn320LysfsTer30
ENST00000648758.1:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT	ENSP00000497731.1:p.Asn320LysfsTer30
ENST00000649902.1:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT	ENSP00000497216.1:p.Asn320LysfsTer30
ENST00000374855.8:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT	ENSP00000363988.4:p.Asn320LysfsTer30
ENST00000616752.1:c.922_923insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT	ENSP00000481363.1:p.Thr308SerfsTer35
NM_000035.3:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT	NP_000026.2:p.Asn320LysfsTer30
NM_000035.4:c.959_960insGCCCCGAGCGAATCCGTCGCCTCCTCGTGACAGACGAAGGCCACCCCAGCCTCGTCCGT MANE Select	NP_000026.2:p.Asn320LysfsTer30