Canonical Allele Identifier: CA2691007041

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101425185-TGCTTTTGCTGAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425186_101425198del , CM000671.2:g.101425186_101425198del	GRCh38
NC_000009.11:g.104187468_104187480del , CM000671.1:g.104187468_104187480del	GRCh37
NC_000009.10:g.103227289_103227301del	NCBI36
NG_012387.1:g.15583_15595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.800-156_800-144del MANE Select	ENSP00000497767.1:n.800-156_800-144del
ENST00000648064.1:c.800-156_800-144del	ENSP00000497990.1:n.800-156_800-144del
ENST00000648758.1:c.800-156_800-144del	ENSP00000497731.1:n.800-156_800-144del
ENST00000649902.1:c.800-156_800-144del	ENSP00000497216.1:n.800-156_800-144del
ENST00000374855.8:c.800-156_800-144del	ENSP00000363988.4:n.800-156_800-144del
ENST00000616752.1:c.800-156_800-144del	ENSP00000481363.1:n.800-156_800-144del
NM_000035.3:c.800-156_800-144del	NP_000026.2:n.800-156_800-144del
NM_000035.4:c.800-156_800-144del MANE Select	NP_000026.2:n.800-156_800-144del