Canonical Allele Identifier: CA374265647
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429766C>T , CM000671.2:g.101429766C>T GRCh38
NC_000009.11:g.104192048C>T , CM000671.1:g.104192048C>T GRCh37
NC_000009.10:g.103231869C>T NCBI36
NG_012387.1:g.11015G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.313G>A MANE Select ENSP00000497767.1:p.Val105Met
ENST00000648064.1:c.313G>A ENSP00000497990.1:p.Val105Met
ENST00000648758.1:c.313G>A ENSP00000497731.1:p.Val105Met
ENST00000648906.1:n.483G>A
ENST00000649902.1:c.313G>A ENSP00000497216.1:p.Val105Met
ENST00000650613.1:n.389G>A
ENST00000374855.8:c.313G>A ENSP00000363988.4:p.Val105Met
ENST00000468981.3:n.67+43G>A
ENST00000616752.1:c.313G>A ENSP00000481363.1:p.Val105Met
NM_000035.3:c.313G>A NP_000026.2:p.Val105Met
NM_000035.4:c.313G>A MANE Select NP_000026.2:p.Val105Met