Canonical Allele Identifier: CA346474241
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29551264C>G (hg19) chr2:g.29328398C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328398C>G , CM000664.2:g.29328398C>G GRCh38
NC_000002.11:g.29551264C>G , CM000664.1:g.29551264C>G GRCh37
NC_000002.10:g.29404768C>G NCBI36
NG_009445.1:g.598169G>C , LRG_488:g.598169G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1366G>C MANE Select ENSP00000373700.3:p.Asp456His
ENST00000389048.7:c.1366G>C ENSP00000373700.3:p.Asp456His
ENST00000618119.4:c.235G>C ENSP00000482733.1:p.Asp79His
NM_004304.4:c.1366G>C NP_004295.2:p.Asp456His
XR_939920.1:n.706C>G
XR_939921.1:n.680+5870C>G
XR_001738688.2:n.2296G>C
XR_939920.2:n.596C>G
XR_939921.2:n.576+5870C>G
NM_004304.5:c.1366G>C MANE Select NP_004295.2:p.Asp456His
Search 100 bp 5'
Search 100 bp 3'