Canonical Allele Identifier: CA1868281053
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429676G= , CM000671.2:g.101429676G= GRCh38
NC_000009.11:g.104191958G= , CM000671.1:g.104191958G= GRCh37
NC_000009.10:g.103231779G= NCBI36
NG_012387.1:g.11105C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.324+79C= MANE Select ENSP00000497767.1:n.324+79C=
ENST00000648064.1:c.324+79C= ENSP00000497990.1:n.324+79C=
ENST00000648758.1:c.324+79C= ENSP00000497731.1:n.324+79C=
ENST00000648906.1:n.573C=
ENST00000649902.1:c.324+79C= ENSP00000497216.1:n.324+79C=
ENST00000650613.1:n.479C=
ENST00000374855.8:c.324+79C= ENSP00000363988.4:n.324+79C=
ENST00000468981.3:n.67+133C=
ENST00000616752.1:c.324+79C= ENSP00000481363.1:n.324+79C=
NM_000035.3:c.324+79C= NP_000026.2:n.324+79C=
NM_000035.4:c.324+79C= MANE Select NP_000026.2:n.324+79C=