Canonical Allele Identifier: CA346587611
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29940445A>T (hg19) chr2:g.29717579A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717579A>T , CM000664.2:g.29717579A>T GRCh38
NC_000002.11:g.29940445A>T , CM000664.1:g.29940445A>T GRCh37
NC_000002.10:g.29793949A>T NCBI36
NG_009445.1:g.208988T>A , LRG_488:g.208988T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.786T>A MANE Select ENSP00000373700.3:p.Tyr262Ter
ENST00000389048.7:c.786T>A ENSP00000373700.3:p.Tyr262Ter
ENST00000618119.4:c.-346T>A ENSP00000482733.1:n.-346T>A
NM_004304.4:c.786T>A NP_004295.2:p.Tyr262Ter
XR_001738688.2:n.1716T>A
NM_004304.5:c.786T>A MANE Select NP_004295.2:p.Tyr262Ter
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