Canonical Allele Identifier: CA2528007265
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429856del , CM000671.2:g.101429856del GRCh38
NC_000009.11:g.104192138del , CM000671.1:g.104192138del GRCh37
NC_000009.10:g.103231959del NCBI36
NG_012387.1:g.10929del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.227del MANE Select ENSP00000497767.1:p.Gly76ValfsTer2
ENST00000648064.1:c.227del ENSP00000497990.1:p.Gly76ValfsTer2
ENST00000648758.1:c.227del ENSP00000497731.1:p.Gly76ValfsTer2
ENST00000648906.1:n.397del
ENST00000649902.1:c.227del ENSP00000497216.1:p.Gly76ValfsTer2
ENST00000650613.1:n.303del
ENST00000374855.8:c.227del ENSP00000363988.4:p.Gly76ValfsTer2
ENST00000468981.3:n.24del
ENST00000616752.1:c.227del ENSP00000481363.1:p.Gly76ValfsTer2
NM_000035.3:c.227del NP_000026.2:p.Gly76ValfsTer2
NM_000035.4:c.227del MANE Select NP_000026.2:p.Gly76ValfsTer2