Canonical Allele Identifier: CA1241144849
Gene: ALK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328629A= , CM000664.2:g.29328629A= GRCh38
NC_000002.11:g.29551495A= , CM000664.1:g.29551495A= GRCh37
NC_000002.10:g.29404999A= NCBI36
NG_009445.1:g.597938T= , LRG_488:g.597938T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-148T= MANE Select ENSP00000373700.3:n.1283-148T=
ENST00000389048.7:c.1283-148T= ENSP00000373700.3:n.1283-148T=
ENST00000618119.4:c.152-148T= ENSP00000482733.1:n.152-148T=
NM_004304.4:c.1283-148T= NP_004295.2:n.1283-148T=
XR_939920.1:n.817+120A=
XR_939921.1:n.680+6101A=
XR_001738688.2:n.2213-148T=
XR_939920.2:n.707+120A=
XR_939921.2:n.576+6101A=
NM_004304.5:c.1283-148T= MANE Select NP_004295.2:n.1283-148T=
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