Canonical Allele Identifier: CA2579403771

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101430737-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430740_101430741del , CM000671.2:g.101430740_101430741del	GRCh38
NC_000009.11:g.104193022_104193023del , CM000671.1:g.104193022_104193023del	GRCh37
NC_000009.10:g.103232843_103232844del	NCBI36
NG_012387.1:g.10042_10043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.112+37_112+38del MANE Select	ENSP00000497767.1:n.112+37_112+38del
ENST00000648064.1:c.112+37_112+38del	ENSP00000497990.1:n.112+37_112+38del
ENST00000648423.1:c.112+37_112+38del	ENSP00000497985.1:n.112+37_112+38del
ENST00000648758.1:c.112+37_112+38del	ENSP00000497731.1:n.112+37_112+38del
ENST00000648906.1:n.282+37_282+38del
ENST00000649902.1:c.112+37_112+38del	ENSP00000497216.1:n.112+37_112+38del
ENST00000650613.1:n.188+37_188+38del
ENST00000374855.8:c.112+37_112+38del	ENSP00000363988.4:n.112+37_112+38del
ENST00000616752.1:c.112+37_112+38del	ENSP00000481363.1:n.112+37_112+38del
NM_000035.3:c.112+37_112+38del	NP_000026.2:n.112+37_112+38del
NM_000035.4:c.112+37_112+38del MANE Select	NP_000026.2:n.112+37_112+38del