Canonical Allele Identifier: CA1868278486

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424897A= , CM000671.2:g.101424897A=	GRCh38
NC_000009.11:g.104187179A= , CM000671.1:g.104187179A=	GRCh37
NC_000009.10:g.103227000A=	NCBI36
NG_012387.1:g.15884T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.945T= MANE Select	ENSP00000497767.1:p.Gly315=
ENST00000648064.1:c.945T=	ENSP00000497990.1:p.Gly315=
ENST00000648758.1:c.945T=	ENSP00000497731.1:p.Gly315=
ENST00000649902.1:c.945T=	ENSP00000497216.1:p.Gly315=
ENST00000374855.8:c.945T=	ENSP00000363988.4:p.Gly315=
ENST00000616752.1:c.908T=	ENSP00000481363.1:p.Val303=
NM_000035.3:c.945T=	NP_000026.2:p.Gly315=
NM_000035.4:c.945T= MANE Select	NP_000026.2:p.Gly315=