Canonical Allele Identifier: CA1241144698
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328489_29328491delinsGCA , CM000664.2:g.29328489_29328491delinsGCA GRCh38
NC_000002.11:g.29551355_29551357delinsGCA , CM000664.1:g.29551355_29551357delinsGCA GRCh37
NC_000002.10:g.29404859_29404861delinsGCA NCBI36
NG_009445.1:g.598076_598078delinsTGC , LRG_488:g.598076_598078delinsTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-10_1283-8delinsTGC MANE Select ENSP00000373700.3:n.1283-10_1283-8delinsT...
ENST00000389048.7:c.1283-10_1283-8delinsTGC ENSP00000373700.3:n.1283-10_1283-8delinsT...
ENST00000618119.4:c.152-10_152-8delinsTGC ENSP00000482733.1:n.152-10_152-8delinsTGC...
NM_004304.4:c.1283-10_1283-8delinsTGC NP_004295.2:n.1283-10_1283-8delinsTGC
XR_939920.1:n.797_799delinsGCA
XR_939921.1:n.680+5961_680+5963delinsGCA
XR_001738688.2:n.2213-10_2213-8delinsTGC
XR_939920.2:n.687_689delinsGCA
XR_939921.2:n.576+5961_576+5963delinsGCA
NM_004304.5:c.1283-10_1283-8delinsTGC MANE Select NP_004295.2:n.1283-10_1283-8delinsTGC