Canonical Allele Identifier: CA2658461731
Gene: ALK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29220776del , CM000664.2:g.29220776del GRCh38
NC_000002.11:g.29443642del , CM000664.1:g.29443642del GRCh37
NC_000002.10:g.29297146del NCBI36
NG_009445.1:g.705792del , LRG_488:g.705792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3576del MANE Select ENSP00000373700.3:p.Phe1193SerfsTer?
ENST00000431873.6:c.803del
ENST00000638605.1:n.453del
ENST00000642122.1:c.372del ENSP00000493203.1:p.Phe125SerfsTer?
ENST00000389048.7:c.3576del ENSP00000373700.3:p.Phe1193SerfsTer?
ENST00000431873.5:c.456del ENSP00000414027.2:p.Phe153SerfsTer?
ENST00000618119.4:c.2445del ENSP00000482733.1:p.Phe816SerfsTer?
NM_004304.4:c.3576del NP_004295.2:p.Phe1193SerfsTer?
NM_001353765.1:c.372del NP_001340694.1:p.Phe125SerfsTer?
XM_024452778.1:c.729del XP_024308546.1:p.Phe244SerfsTer?
XM_024452779.1:c.372del XP_024308547.1:p.Phe125SerfsTer?
NM_004304.5:c.3576del MANE Select NP_004295.2:p.Phe1193SerfsTer?
NM_001353765.2:c.372del NP_001340694.1:p.Phe125SerfsTer?