Canonical Allele Identifier: CA653204484

Gene: ALDOB

Linked Data

• COSMIC: COSN5117301

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428458A>G , CM000671.2:g.101428458A>G	GRCh38
NC_000009.11:g.104190740A>G , CM000671.1:g.104190740A>G	GRCh37
NC_000009.10:g.103230561A>G	NCBI36
NG_012387.1:g.12323T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.379+11T>C MANE Select	ENSP00000497767.1:n.379+11T>C
ENST00000648064.1:c.379+11T>C	ENSP00000497990.1:n.379+11T>C
ENST00000648758.1:c.379+11T>C	ENSP00000497731.1:n.379+11T>C
ENST00000649902.1:c.379+11T>C	ENSP00000497216.1:n.379+11T>C
ENST00000374855.8:c.379+11T>C	ENSP00000363988.4:n.379+11T>C
ENST00000468981.3:n.67+1351T>C
ENST00000616752.1:c.379+11T>C	ENSP00000481363.1:n.379+11T>C
NM_000035.3:c.379+11T>C	NP_000026.2:n.379+11T>C
NM_000035.4:c.379+11T>C MANE Select	NP_000026.2:n.379+11T>C