Canonical Allele Identifier: CA1868280965

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429469_101429470delinsTA , CM000671.2:g.101429469_101429470delinsTA	GRCh38
NC_000009.11:g.104191751_104191752delinsTA , CM000671.1:g.104191751_104191752delinsTA	GRCh37
NC_000009.10:g.103231572_103231573delinsTA	NCBI36
NG_012387.1:g.11311_11312delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+285_324+286delinsTA MANE Select	ENSP00000497767.1:n.324+285_324+286delinsTA
ENST00000648064.1:c.324+285_324+286delinsTA	ENSP00000497990.1:n.324+285_324+286delinsTA
ENST00000648758.1:c.324+285_324+286delinsTA	ENSP00000497731.1:n.324+285_324+286delinsTA
ENST00000648906.1:n.779_780delinsTA
ENST00000649902.1:c.324+285_324+286delinsTA	ENSP00000497216.1:n.324+285_324+286delinsTA
ENST00000650613.1:n.685_686delinsTA
ENST00000374855.8:c.324+285_324+286delinsTA	ENSP00000363988.4:n.324+285_324+286delinsTA
ENST00000468981.3:n.67+339_67+340delinsTA
ENST00000616752.1:c.324+285_324+286delinsTA	ENSP00000481363.1:n.324+285_324+286delinsTA
NM_000035.3:c.324+285_324+286delinsTA	NP_000026.2:n.324+285_324+286delinsTA
NM_000035.4:c.324+285_324+286delinsTA MANE Select	NP_000026.2:n.324+285_324+286delinsTA