Canonical Allele Identifier: CA1868281013

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429571_101429572delinsAG , CM000671.2:g.101429571_101429572delinsAG	GRCh38
NC_000009.11:g.104191853_104191854delinsAG , CM000671.1:g.104191853_104191854delinsAG	GRCh37
NC_000009.10:g.103231674_103231675delinsAG	NCBI36
NG_012387.1:g.11209_11210delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+183_324+184delinsCT MANE Select	ENSP00000497767.1:n.324+183_324+184delinsCT
ENST00000648064.1:c.324+183_324+184delinsCT	ENSP00000497990.1:n.324+183_324+184delinsCT
ENST00000648758.1:c.324+183_324+184delinsCT	ENSP00000497731.1:n.324+183_324+184delinsCT
ENST00000648906.1:n.677_678delinsCT
ENST00000649902.1:c.324+183_324+184delinsCT	ENSP00000497216.1:n.324+183_324+184delinsCT
ENST00000650613.1:n.583_584delinsCT
ENST00000374855.8:c.324+183_324+184delinsCT	ENSP00000363988.4:n.324+183_324+184delinsCT
ENST00000468981.3:n.67+237_67+238delinsCT
ENST00000616752.1:c.324+183_324+184delinsCT	ENSP00000481363.1:n.324+183_324+184delinsCT
NM_000035.3:c.324+183_324+184delinsCT	NP_000026.2:n.324+183_324+184delinsCT
NM_000035.4:c.324+183_324+184delinsCT MANE Select	NP_000026.2:n.324+183_324+184delinsCT