Canonical Allele Identifier: CA1868281031

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429626_101429629delinsTGAC , CM000671.2:g.101429626_101429629delinsTGAC	GRCh38
NC_000009.11:g.104191908_104191911delinsTGAC , CM000671.1:g.104191908_104191911delinsTGAC	GRCh37
NC_000009.10:g.103231729_103231732delinsTGAC	NCBI36
NG_012387.1:g.11152_11155delinsGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+126_324+129delinsGTCA MANE Select	ENSP00000497767.1:n.324+126_324+129delinsGTCA
ENST00000648064.1:c.324+126_324+129delinsGTCA	ENSP00000497990.1:n.324+126_324+129delinsGTCA
ENST00000648758.1:c.324+126_324+129delinsGTCA	ENSP00000497731.1:n.324+126_324+129delinsGTCA
ENST00000648906.1:n.620_623delinsGTCA
ENST00000649902.1:c.324+126_324+129delinsGTCA	ENSP00000497216.1:n.324+126_324+129delinsGTCA
ENST00000650613.1:n.526_529delinsGTCA
ENST00000374855.8:c.324+126_324+129delinsGTCA	ENSP00000363988.4:n.324+126_324+129delinsGTCA
ENST00000468981.3:n.67+180_67+183delinsGTCA
ENST00000616752.1:c.324+126_324+129delinsGTCA	ENSP00000481363.1:n.324+126_324+129delinsGTCA
NM_000035.3:c.324+126_324+129delinsGTCA	NP_000026.2:n.324+126_324+129delinsGTCA
NM_000035.4:c.324+126_324+129delinsGTCA MANE Select	NP_000026.2:n.324+126_324+129delinsGTCA