Canonical Allele Identifier: CA1241144898
Gene: ALK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328673G= , CM000664.2:g.29328673G= GRCh38
NC_000002.11:g.29551539G= , CM000664.1:g.29551539G= GRCh37
NC_000002.10:g.29405043G= NCBI36
NG_009445.1:g.597894C= , LRG_488:g.597894C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-192C= MANE Select ENSP00000373700.3:n.1283-192C=
ENST00000389048.7:c.1283-192C= ENSP00000373700.3:n.1283-192C=
ENST00000618119.4:c.152-192C= ENSP00000482733.1:n.152-192C=
NM_004304.4:c.1283-192C= NP_004295.2:n.1283-192C=
XR_939920.1:n.817+164G=
XR_939921.1:n.680+6145G=
XR_001738688.2:n.2213-192C=
XR_939920.2:n.707+164G=
XR_939921.2:n.576+6145G=
NM_004304.5:c.1283-192C= MANE Select NP_004295.2:n.1283-192C=
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