Canonical Allele Identifier: CA2691007430

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101427388-G-GGAGGTCCATTTGTAGTTATAGTATAATTGAAAAGAAAAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427389_101427428dup , CM000671.2:g.101427389_101427428dup	GRCh38
NC_000009.11:g.104189671_104189710dup , CM000671.1:g.104189671_104189710dup	GRCh37
NC_000009.10:g.103229492_103229531dup	NCBI36
NG_012387.1:g.13353_13392dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.540+54_540+93dup MANE Select	ENSP00000497767.1:n.540+54_540+93dup
ENST00000648064.1:c.540+54_540+93dup	ENSP00000497990.1:n.540+54_540+93dup
ENST00000648758.1:c.540+54_540+93dup	ENSP00000497731.1:n.540+54_540+93dup
ENST00000649902.1:c.540+54_540+93dup	ENSP00000497216.1:n.540+54_540+93dup
ENST00000374855.8:c.540+54_540+93dup	ENSP00000363988.4:n.540+54_540+93dup
ENST00000468981.3:n.68-790_68-751dup
ENST00000616752.1:c.540+54_540+93dup	ENSP00000481363.1:n.540+54_540+93dup
NM_000035.3:c.540+54_540+93dup	NP_000026.2:n.540+54_540+93dup
NM_000035.4:c.540+54_540+93dup MANE Select	NP_000026.2:n.540+54_540+93dup