Canonical Allele Identifier: CA915943720

Gene: ALK

Linked Data

• ClinVar Variation Id: 707089
• ClinVar RCV Id: RCV002539255
• dbSNP Id: rs1573239381

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328494_29328495del , CM000664.2:g.29328494_29328495del	GRCh38
NC_000002.11:g.29551360_29551361del , CM000664.1:g.29551360_29551361del	GRCh37
NC_000002.10:g.29404864_29404865del	NCBI36
NG_009445.1:g.598076_598077del , LRG_488:g.598076_598077del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1283-10_1283-9del MANE Select	ENSP00000373700.3:n.1283-10_1283-9del
ENST00000389048.7:c.1283-10_1283-9del	ENSP00000373700.3:n.1283-10_1283-9del
ENST00000618119.4:c.152-10_152-9del	ENSP00000482733.1:n.152-10_152-9del
NM_004304.4:c.1283-10_1283-9del	NP_004295.2:n.1283-10_1283-9del
XR_939920.1:n.802_803del
XR_939921.1:n.680+5966_680+5967del
XR_001738688.2:n.2213-10_2213-9del
XR_939920.2:n.692_693del
XR_939921.2:n.576+5966_576+5967del
NM_004304.5:c.1283-10_1283-9del MANE Select	NP_004295.2:n.1283-10_1283-9del