Canonical Allele Identifier: CA2580066338

Gene: ALK

Linked Data

• ClinVar Variation Id: 2022776
• ClinVar RCV Id: RCV002875687

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220801del , CM000664.2:g.29220801del	GRCh38
NC_000002.11:g.29443667del , CM000664.1:g.29443667del	GRCh37
NC_000002.10:g.29297171del	NCBI36
NG_009445.1:g.705769del , LRG_488:g.705769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3553del MANE Select	ENSP00000373700.3:p.Val1185Ter
ENST00000431873.6:c.780del
ENST00000638605.1:n.430del
ENST00000642122.1:c.349del	ENSP00000493203.1:p.Val117Ter
ENST00000389048.7:c.3553del	ENSP00000373700.3:p.Val1185Ter
ENST00000431873.5:c.433del	ENSP00000414027.2:p.Val145Ter
ENST00000618119.4:c.2422del	ENSP00000482733.1:p.Val808Ter
NM_004304.4:c.3553del	NP_004295.2:p.Val1185Ter
NM_001353765.1:c.349del	NP_001340694.1:p.Val117Ter
XM_024452778.1:c.706del	XP_024308546.1:p.Val236Ter
XM_024452779.1:c.349del	XP_024308547.1:p.Val117Ter
NM_004304.5:c.3553del MANE Select	NP_004295.2:p.Val1185Ter
NM_001353765.2:c.349del	NP_001340694.1:p.Val117Ter