Canonical Allele Identifier: CA1868281200

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429954T= , CM000671.2:g.101429954T=	GRCh38
NC_000009.11:g.104192236T= , CM000671.1:g.104192236T=	GRCh37
NC_000009.10:g.103232057T=	NCBI36
NG_012387.1:g.10827A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.125A= MANE Select	ENSP00000497767.1:p.Asn42=
ENST00000648064.1:c.125A=	ENSP00000497990.1:p.Asn42=
ENST00000648423.1:c.125A=	ENSP00000497985.1:p.Asn42=
ENST00000648758.1:c.125A=	ENSP00000497731.1:p.Asn42=
ENST00000648906.1:n.295A=
ENST00000649902.1:c.125A=	ENSP00000497216.1:p.Asn42=
ENST00000650613.1:n.201A=
ENST00000374855.8:c.125A=	ENSP00000363988.4:p.Asn42=
ENST00000616752.1:c.125A=	ENSP00000481363.1:p.Asn42=
NM_000035.3:c.125A=	NP_000026.2:p.Asn42=
NM_000035.4:c.125A= MANE Select	NP_000026.2:p.Asn42=