Canonical Allele Identifier: CA1868281081

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429749G= , CM000671.2:g.101429749G=	GRCh38
NC_000009.11:g.104192031G= , CM000671.1:g.104192031G=	GRCh37
NC_000009.10:g.103231852G=	NCBI36
NG_012387.1:g.11032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+6C= MANE Select	ENSP00000497767.1:n.324+6C=
ENST00000648064.1:c.324+6C=	ENSP00000497990.1:n.324+6C=
ENST00000648758.1:c.324+6C=	ENSP00000497731.1:n.324+6C=
ENST00000648906.1:n.500C=
ENST00000649902.1:c.324+6C=	ENSP00000497216.1:n.324+6C=
ENST00000650613.1:n.406C=
ENST00000374855.8:c.324+6C=	ENSP00000363988.4:n.324+6C=
ENST00000468981.3:n.67+60C=
ENST00000616752.1:c.324+6C=	ENSP00000481363.1:n.324+6C=
NM_000035.3:c.324+6C=	NP_000026.2:n.324+6C=
NM_000035.4:c.324+6C= MANE Select	NP_000026.2:n.324+6C=