Canonical Allele Identifier: CA2691006958

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101425128-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425128T>A , CM000671.2:g.101425128T>A	GRCh38
NC_000009.11:g.104187410T>A , CM000671.1:g.104187410T>A	GRCh37
NC_000009.10:g.103227231T>A	NCBI36
NG_012387.1:g.15653A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.800-86A>T MANE Select	ENSP00000497767.1:n.800-86A>T
ENST00000648064.1:c.800-86A>T	ENSP00000497990.1:n.800-86A>T
ENST00000648758.1:c.800-86A>T	ENSP00000497731.1:n.800-86A>T
ENST00000649902.1:c.800-86A>T	ENSP00000497216.1:n.800-86A>T
ENST00000374855.8:c.800-86A>T	ENSP00000363988.4:n.800-86A>T
ENST00000616752.1:c.800-86A>T	ENSP00000481363.1:n.800-86A>T
NM_000035.3:c.800-86A>T	NP_000026.2:n.800-86A>T
NM_000035.4:c.800-86A>T MANE Select	NP_000026.2:n.800-86A>T