Canonical Allele Identifier: CA2691007446

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101427422-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427425_101427426del , CM000671.2:g.101427425_101427426del	GRCh38
NC_000009.11:g.104189707_104189708del , CM000671.1:g.104189707_104189708del	GRCh37
NC_000009.10:g.103229528_103229529del	NCBI36
NG_012387.1:g.13357_13358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.540+58_540+59del MANE Select	ENSP00000497767.1:n.540+58_540+59del
ENST00000648064.1:c.540+58_540+59del	ENSP00000497990.1:n.540+58_540+59del
ENST00000648758.1:c.540+58_540+59del	ENSP00000497731.1:n.540+58_540+59del
ENST00000649902.1:c.540+58_540+59del	ENSP00000497216.1:n.540+58_540+59del
ENST00000374855.8:c.540+58_540+59del	ENSP00000363988.4:n.540+58_540+59del
ENST00000468981.3:n.68-786_68-785del
ENST00000616752.1:c.540+58_540+59del	ENSP00000481363.1:n.540+58_540+59del
NM_000035.3:c.540+58_540+59del	NP_000026.2:n.540+58_540+59del
NM_000035.4:c.540+58_540+59del MANE Select	NP_000026.2:n.540+58_540+59del