All variants in the ALK gene

Information The variants shown are described using the NM_004304.4 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/. - c.3452C>T r.(?) p.(Thr1151Met) - pathogenic g.29445273G>A g.29222407G>A - - ALK_000087 risk factor; 80 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs113994091 Germline - 80/2795 individuals - 0 - Mohammed Faruq
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