Canonical Allele Identifier: CA1868280960

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429465_101429466delinsCT , CM000671.2:g.101429465_101429466delinsCT	GRCh38
NC_000009.11:g.104191747_104191748delinsCT , CM000671.1:g.104191747_104191748delinsCT	GRCh37
NC_000009.10:g.103231568_103231569delinsCT	NCBI36
NG_012387.1:g.11315_11316delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+289_324+290delinsAG MANE Select	ENSP00000497767.1:n.324+289_324+290delinsAG
ENST00000648064.1:c.324+289_324+290delinsAG	ENSP00000497990.1:n.324+289_324+290delinsAG
ENST00000648758.1:c.324+289_324+290delinsAG	ENSP00000497731.1:n.324+289_324+290delinsAG
ENST00000648906.1:n.783_784delinsAG
ENST00000649902.1:c.324+289_324+290delinsAG	ENSP00000497216.1:n.324+289_324+290delinsAG
ENST00000650613.1:n.689_690delinsAG
ENST00000374855.8:c.324+289_324+290delinsAG	ENSP00000363988.4:n.324+289_324+290delinsAG
ENST00000468981.3:n.67+343_67+344delinsAG
ENST00000616752.1:c.324+289_324+290delinsAG	ENSP00000481363.1:n.324+289_324+290delinsAG
NM_000035.3:c.324+289_324+290delinsAG	NP_000026.2:n.324+289_324+290delinsAG
NM_000035.4:c.324+289_324+290delinsAG MANE Select	NP_000026.2:n.324+289_324+290delinsAG