Canonical Allele Identifier: CA1868280991

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429528_101429529delinsTG , CM000671.2:g.101429528_101429529delinsTG	GRCh38
NC_000009.11:g.104191810_104191811delinsTG , CM000671.1:g.104191810_104191811delinsTG	GRCh37
NC_000009.10:g.103231631_103231632delinsTG	NCBI36
NG_012387.1:g.11252_11253delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+226_324+227delinsCA MANE Select	ENSP00000497767.1:n.324+226_324+227delinsCA
ENST00000648064.1:c.324+226_324+227delinsCA	ENSP00000497990.1:n.324+226_324+227delinsCA
ENST00000648758.1:c.324+226_324+227delinsCA	ENSP00000497731.1:n.324+226_324+227delinsCA
ENST00000648906.1:n.720_721delinsCA
ENST00000649902.1:c.324+226_324+227delinsCA	ENSP00000497216.1:n.324+226_324+227delinsCA
ENST00000650613.1:n.626_627delinsCA
ENST00000374855.8:c.324+226_324+227delinsCA	ENSP00000363988.4:n.324+226_324+227delinsCA
ENST00000468981.3:n.67+280_67+281delinsCA
ENST00000616752.1:c.324+226_324+227delinsCA	ENSP00000481363.1:n.324+226_324+227delinsCA
NM_000035.3:c.324+226_324+227delinsCA	NP_000026.2:n.324+226_324+227delinsCA
NM_000035.4:c.324+226_324+227delinsCA MANE Select	NP_000026.2:n.324+226_324+227delinsCA