Canonical Allele Identifier: CA1868281217
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429975G= , CM000671.2:g.101429975G= GRCh38
NC_000009.11:g.104192257G= , CM000671.1:g.104192257G= GRCh37
NC_000009.10:g.103232078G= NCBI36
NG_012387.1:g.10806C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.113-9C= MANE Select ENSP00000497767.1:n.113-9C=
ENST00000648064.1:c.113-9C= ENSP00000497990.1:n.113-9C=
ENST00000648423.1:c.113-9C= ENSP00000497985.1:n.113-9C=
ENST00000648758.1:c.113-9C= ENSP00000497731.1:n.113-9C=
ENST00000648906.1:n.283-9C=
ENST00000649902.1:c.113-9C= ENSP00000497216.1:n.113-9C=
ENST00000650613.1:n.189-9C=
ENST00000374855.8:c.113-9C= ENSP00000363988.4:n.113-9C=
ENST00000616752.1:c.113-9C= ENSP00000481363.1:n.113-9C=
NM_000035.3:c.113-9C= NP_000026.2:n.113-9C=
NM_000035.4:c.113-9C= MANE Select NP_000026.2:n.113-9C=