Canonical Allele Identifier: CA2523669536
Gene: ALK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328488A>C , CM000664.2:g.29328488A>C GRCh38
NC_000002.11:g.29551354A>C , CM000664.1:g.29551354A>C GRCh37
NC_000002.10:g.29404858A>C NCBI36
NG_009445.1:g.598079T>G , LRG_488:g.598079T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-7T>G MANE Select ENSP00000373700.3:n.1283-7T>G
ENST00000389048.7:c.1283-7T>G ENSP00000373700.3:n.1283-7T>G
ENST00000618119.4:c.152-7T>G ENSP00000482733.1:n.152-7T>G
NM_004304.4:c.1283-7T>G NP_004295.2:n.1283-7T>G
XR_939920.1:n.796A>C
XR_939921.1:n.680+5960A>C
XR_001738688.2:n.2213-7T>G
XR_939920.2:n.686A>C
XR_939921.2:n.576+5960A>C
NM_004304.5:c.1283-7T>G MANE Select NP_004295.2:n.1283-7T>G
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