Canonical Allele Identifier: CA1868278811
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425167_101425176delinsCAAACTGAGA , CM000671.2:g.101425167_101425176delinsCAAACTGAGA GRCh38
NC_000009.11:g.104187449_104187458delinsCAAACTGAGA , CM000671.1:g.104187449_104187458delinsCAAACTGAGA GRCh37
NC_000009.10:g.103227270_103227279delinsCAAACTGAGA NCBI36
NG_012387.1:g.15605_15614delinsTCTCAGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.800-134_800-125delinsTCTCAGTTTG MANE Select ENSP00000497767.1:n.800-134_800-125delinsTCTCAGTTTG
ENST00000648064.1:c.800-134_800-125delinsTCTCAGTTTG ENSP00000497990.1:n.800-134_800-125delinsTCTCAGTTTG
ENST00000648758.1:c.800-134_800-125delinsTCTCAGTTTG ENSP00000497731.1:n.800-134_800-125delinsTCTCAGTTTG
ENST00000649902.1:c.800-134_800-125delinsTCTCAGTTTG ENSP00000497216.1:n.800-134_800-125delinsTCTCAGTTTG
ENST00000374855.8:c.800-134_800-125delinsTCTCAGTTTG ENSP00000363988.4:n.800-134_800-125delinsTCTCAGTTTG
ENST00000616752.1:c.800-134_800-125delinsTCTCAGTTTG ENSP00000481363.1:n.800-134_800-125delinsTCTCAGTTTG
NM_000035.3:c.800-134_800-125delinsTCTCAGTTTG NP_000026.2:n.800-134_800-125delinsTCTCAGTTTG
NM_000035.4:c.800-134_800-125delinsTCTCAGTTTG MANE Select NP_000026.2:n.800-134_800-125delinsTCTCAGTTTG