Canonical Allele Identifier: CA3018839162

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101435667A>T , CM000671.2:g.101435667A>T	GRCh38
NC_000009.11:g.104197949A>T , CM000671.1:g.104197949A>T	GRCh37
NC_000009.10:g.103237770A>T	NCBI36
NG_012387.1:g.5114T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000035.4:c.-11+42T>A MANE Select	NP_000026.2:n.-11+42T>A
ENST00000647789.2:c.-11+42T>A MANE Select	ENSP00000497767.1:n.-11+42T>A
NM_000035.3:c.-11+42T>A	NP_000026.2:n.-11+42T>A
ENST00000374855.8:c.-11+42T>A	ENSP00000363988.4:n.-11+42T>A
ENST00000616752.1:c.-11+42T>A	ENSP00000481363.1:n.-11+42T>A
ENST00000648064.1:c.-10-4770T>A	ENSP00000497990.1:n.-10-4770T>A
ENST00000648423.1:c.-11+42T>A	ENSP00000497985.1:n.-11+42T>A
ENST00000648758.1:c.-10-4770T>A	ENSP00000497731.1:n.-10-4770T>A
ENST00000650613.1:n.66+42T>A