Canonical Allele Identifier: CA425521654
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29940448T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717582T>C , CM000664.2:g.29717582T>C GRCh38
NC_000002.11:g.29940448T>C , CM000664.1:g.29940448T>C GRCh37
NC_000002.10:g.29793952T>C NCBI36
NG_009445.1:g.208985A>G , LRG_488:g.208985A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.783A>G MANE Select ENSP00000373700.3:p.Arg261=
ENST00000389048.7:c.783A>G ENSP00000373700.3:p.Arg261=
ENST00000618119.4:c.-349A>G ENSP00000482733.1:n.-349A>G
NM_004304.4:c.783A>G NP_004295.2:p.Arg261=
XR_001738688.2:n.1713A>G
NM_004304.5:c.783A>G MANE Select NP_004295.2:p.Arg261=
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Search 100 bp 3'