Canonical Allele Identifier: CA1868281623

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430799A= , CM000671.2:g.101430799A=	GRCh38
NC_000009.11:g.104193081A= , CM000671.1:g.104193081A=	GRCh37
NC_000009.10:g.103232902A=	NCBI36
NG_012387.1:g.9982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.89T= MANE Select	ENSP00000497767.1:p.Ile30=
ENST00000648064.1:c.89T=	ENSP00000497990.1:p.Ile30=
ENST00000648423.1:c.89T=	ENSP00000497985.1:p.Ile30=
ENST00000648758.1:c.89T=	ENSP00000497731.1:p.Ile30=
ENST00000648906.1:n.259T=
ENST00000649902.1:c.89T=	ENSP00000497216.1:p.Ile30=
ENST00000650613.1:n.165T=
ENST00000374855.8:c.89T=	ENSP00000363988.4:p.Ile30=
ENST00000616752.1:c.89T=	ENSP00000481363.1:p.Ile30=
NM_000035.3:c.89T=	NP_000026.2:p.Ile30=
NM_000035.4:c.89T= MANE Select	NP_000026.2:p.Ile30=