Canonical Allele Identifier: CA2576925734
Gene: ALK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328513A>G , CM000664.2:g.29328513A>G GRCh38
NC_000002.11:g.29551379A>G , CM000664.1:g.29551379A>G GRCh37
NC_000002.10:g.29404883A>G NCBI36
NG_009445.1:g.598054T>C , LRG_488:g.598054T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-32T>C MANE Select ENSP00000373700.3:n.1283-32T>C
ENST00000389048.7:c.1283-32T>C ENSP00000373700.3:n.1283-32T>C
ENST00000618119.4:c.152-32T>C ENSP00000482733.1:n.152-32T>C
NM_004304.4:c.1283-32T>C NP_004295.2:n.1283-32T>C
XR_939920.1:n.817+4A>G
XR_939921.1:n.680+5985A>G
XR_001738688.2:n.2213-32T>C
XR_939920.2:n.707+4A>G
XR_939921.2:n.576+5985A>G
NM_004304.5:c.1283-32T>C MANE Select NP_004295.2:n.1283-32T>C
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