Canonical Allele Identifier: CA1241144940
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667350693

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328744_29328751del , CM000664.2:g.29328744_29328751del GRCh38
NC_000002.11:g.29551610_29551617del , CM000664.1:g.29551610_29551617del GRCh37
NC_000002.10:g.29405114_29405121del NCBI36
NG_009445.1:g.597816_597823del , LRG_488:g.597816_597823del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-270_1283-263del MANE Select ENSP00000373700.3:n.1283-270_1283-263del
ENST00000389048.7:c.1283-270_1283-263del ENSP00000373700.3:n.1283-270_1283-263del
ENST00000618119.4:c.152-270_152-263del ENSP00000482733.1:n.152-270_152-263del
NM_004304.4:c.1283-270_1283-263del NP_004295.2:n.1283-270_1283-263del
XR_939920.1:n.818-181_818-174del
XR_939921.1:n.680+6216_680+6223del
XR_001738688.2:n.2213-270_2213-263del
XR_939920.2:n.708-181_708-174del
XR_939921.2:n.576+6216_576+6223del
NM_004304.5:c.1283-270_1283-263del MANE Select NP_004295.2:n.1283-270_1283-263del