Canonical Allele Identifier: CA1868280499

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428468C= , CM000671.2:g.101428468C=	GRCh38
NC_000009.11:g.104190750C= , CM000671.1:g.104190750C=	GRCh37
NC_000009.10:g.103230571C=	NCBI36
NG_012387.1:g.12313G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.379+1G= MANE Select	ENSP00000497767.1:n.379+1G=
ENST00000648064.1:c.379+1G=	ENSP00000497990.1:n.379+1G=
ENST00000648758.1:c.379+1G=	ENSP00000497731.1:n.379+1G=
ENST00000649902.1:c.379+1G=	ENSP00000497216.1:n.379+1G=
ENST00000374855.8:c.379+1G=	ENSP00000363988.4:n.379+1G=
ENST00000468981.3:n.67+1341G=
ENST00000616752.1:c.379+1G=	ENSP00000481363.1:n.379+1G=
NM_000035.3:c.379+1G=	NP_000026.2:n.379+1G=
NM_000035.4:c.379+1G= MANE Select	NP_000026.2:n.379+1G=