Canonical Allele Identifier: CA2691006761

Gene: ALDOB

Linked Data

• gnomAD v4: 9-101424894-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424896del , CM000671.2:g.101424896del	GRCh38
NC_000009.11:g.104187178del , CM000671.1:g.104187178del	GRCh37
NC_000009.10:g.103226999del	NCBI36
NG_012387.1:g.15886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.947del MANE Select	ENSP00000497767.1:p.Gly316AlafsTer14
ENST00000648064.1:c.947del	ENSP00000497990.1:p.Gly316AlafsTer14
ENST00000648758.1:c.947del	ENSP00000497731.1:p.Gly316AlafsTer14
ENST00000649902.1:c.947del	ENSP00000497216.1:p.Gly316AlafsTer14
ENST00000374855.8:c.947del	ENSP00000363988.4:p.Gly316AlafsTer14
ENST00000616752.1:c.910del	ENSP00000481363.1:p.Ala304GlnfsTer19
NM_000035.3:c.947del	NP_000026.2:p.Gly316AlafsTer14
NM_000035.4:c.947del MANE Select	NP_000026.2:p.Gly316AlafsTer14