Canonical Allele Identifier: CA346468015
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29449913A>C (hg19) chr2:g.29227047A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227047A>C , CM000664.2:g.29227047A>C GRCh38
NC_000002.11:g.29449913A>C , CM000664.1:g.29449913A>C GRCh37
NC_000002.10:g.29303417A>C NCBI36
NG_009445.1:g.699520T>G , LRG_488:g.699520T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2942T>G MANE Select ENSP00000373700.3:p.Ile981Ser
ENST00000431873.6:c.108T>G
ENST00000389048.7:c.2942T>G ENSP00000373700.3:p.Ile981Ser
ENST00000618119.4:c.1811T>G ENSP00000482733.1:p.Ile604Ser
NM_004304.4:c.2942T>G NP_004295.2:p.Ile981Ser
XM_024452778.1:c.95T>G XP_024308546.1:p.Ile32Ser
XR_001738688.2:n.3798T>G
NM_004304.5:c.2942T>G MANE Select NP_004295.2:p.Ile981Ser
Search 100 bp 5'
Search 100 bp 3'