Canonical Allele Identifier: CA1868281148

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429867T= , CM000671.2:g.101429867T=	GRCh38
NC_000009.11:g.104192149T= , CM000671.1:g.104192149T=	GRCh37
NC_000009.10:g.103231970T=	NCBI36
NG_012387.1:g.10914A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.212A= MANE Select	ENSP00000497767.1:p.Asn71=
ENST00000648064.1:c.212A=	ENSP00000497990.1:p.Asn71=
ENST00000648423.1:c.212A=	ENSP00000497985.1:p.Asn71=
ENST00000648758.1:c.212A=	ENSP00000497731.1:p.Asn71=
ENST00000648906.1:n.382A=
ENST00000649902.1:c.212A=	ENSP00000497216.1:p.Asn71=
ENST00000650613.1:n.288A=
ENST00000374855.8:c.212A=	ENSP00000363988.4:p.Asn71=
ENST00000468981.3:n.9A=
ENST00000616752.1:c.212A=	ENSP00000481363.1:p.Asn71=
NM_000035.3:c.212A=	NP_000026.2:p.Asn71=
NM_000035.4:c.212A= MANE Select	NP_000026.2:p.Asn71=