Canonical Allele Identifier: CA589815636
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1564077839

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101426570_101426575del , CM000671.2:g.101426570_101426575del GRCh38
NC_000009.11:g.104188852_104188857del , CM000671.1:g.104188852_104188857del GRCh37
NC_000009.10:g.103228673_103228678del NCBI36
NG_012387.1:g.14207_14212del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.605_610del MANE Select ENSP00000497767.1:p.Cys202_Gln203del
ENST00000648064.1:c.605_610del ENSP00000497990.1:p.Cys202_Gln203del
ENST00000648758.1:c.605_610del ENSP00000497731.1:p.Cys202_Gln203del
ENST00000649902.1:c.605_610del ENSP00000497216.1:p.Cys202_Gln203del
ENST00000374855.8:c.605_610del ENSP00000363988.4:p.Cys202_Gln203del
ENST00000468981.3:n.132_137del
ENST00000616752.1:c.605_610del ENSP00000481363.1:p.Cys202_Gln203del
NM_000035.3:c.605_610del NP_000026.2:p.Cys202_Gln203del
NM_000035.4:c.605_610del MANE Select NP_000026.2:p.Cys202_Gln203del