Canonical Allele Identifier: CA2691006617

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101430691-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430691T>G , CM000671.2:g.101430691T>G	GRCh38
NC_000009.11:g.104192973T>G , CM000671.1:g.104192973T>G	GRCh37
NC_000009.10:g.103232794T>G	NCBI36
NG_012387.1:g.10090A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.112+85A>C MANE Select	ENSP00000497767.1:n.112+85A>C
ENST00000648064.1:c.112+85A>C	ENSP00000497990.1:n.112+85A>C
ENST00000648423.1:c.112+85A>C	ENSP00000497985.1:n.112+85A>C
ENST00000648758.1:c.112+85A>C	ENSP00000497731.1:n.112+85A>C
ENST00000648906.1:n.282+85A>C
ENST00000649902.1:c.112+85A>C	ENSP00000497216.1:n.112+85A>C
ENST00000650613.1:n.188+85A>C
ENST00000374855.8:c.112+85A>C	ENSP00000363988.4:n.112+85A>C
ENST00000616752.1:c.112+85A>C	ENSP00000481363.1:n.112+85A>C
NM_000035.3:c.112+85A>C	NP_000026.2:n.112+85A>C
NM_000035.4:c.112+85A>C MANE Select	NP_000026.2:n.112+85A>C