Canonical Allele Identifier: CA1241144938
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328743_29328751delinsGGTCCATGT , CM000664.2:g.29328743_29328751delinsGGTCCATGT GRCh38
NC_000002.11:g.29551609_29551617delinsGGTCCATGT , CM000664.1:g.29551609_29551617delinsGGTCCATGT GRCh37
NC_000002.10:g.29405113_29405121delinsGGTCCATGT NCBI36
NG_009445.1:g.597816_597824delinsACATGGACC , LRG_488:g.597816_597824delinsACATGGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-270_1283-262delinsACATGGACC MANE Select ENSP00000373700.3:n.1283-270_1283-262delinsACATGGACC
ENST00000389048.7:c.1283-270_1283-262delinsACATGGACC ENSP00000373700.3:n.1283-270_1283-262delinsACATGGACC
ENST00000618119.4:c.152-270_152-262delinsACATGGACC ENSP00000482733.1:n.152-270_152-262delinsACATGGACC
NM_004304.4:c.1283-270_1283-262delinsACATGGACC NP_004295.2:n.1283-270_1283-262delinsACATGGACC
XR_939920.1:n.818-182_818-174delinsGGTCCATGT
XR_939921.1:n.680+6215_680+6223delinsGGTCCATGT
XR_001738688.2:n.2213-270_2213-262delinsACATGGACC
XR_939920.2:n.708-182_708-174delinsGGTCCATGT
XR_939921.2:n.576+6215_576+6223delinsGGTCCATGT
NM_004304.5:c.1283-270_1283-262delinsACATGGACC MANE Select NP_004295.2:n.1283-270_1283-262delinsACATGGACC