Canonical Allele Identifier: CA1868281589

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430728A= , CM000671.2:g.101430728A=	GRCh38
NC_000009.11:g.104193010A= , CM000671.1:g.104193010A=	GRCh37
NC_000009.10:g.103232831A=	NCBI36
NG_012387.1:g.10053T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.112+48T= MANE Select	ENSP00000497767.1:n.112+48T=
ENST00000648064.1:c.112+48T=	ENSP00000497990.1:n.112+48T=
ENST00000648423.1:c.112+48T=	ENSP00000497985.1:n.112+48T=
ENST00000648758.1:c.112+48T=	ENSP00000497731.1:n.112+48T=
ENST00000648906.1:n.282+48T=
ENST00000649902.1:c.112+48T=	ENSP00000497216.1:n.112+48T=
ENST00000650613.1:n.188+48T=
ENST00000374855.8:c.112+48T=	ENSP00000363988.4:n.112+48T=
ENST00000616752.1:c.112+48T=	ENSP00000481363.1:n.112+48T=
NM_000035.3:c.112+48T=	NP_000026.2:n.112+48T=
NM_000035.4:c.112+48T= MANE Select	NP_000026.2:n.112+48T=