Canonical Allele Identifier: CA346467622
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29449835A>C (hg19) chr2:g.29226969A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29226969A>C , CM000664.2:g.29226969A>C GRCh38
NC_000002.11:g.29449835A>C , CM000664.1:g.29449835A>C GRCh37
NC_000002.10:g.29303339A>C NCBI36
NG_009445.1:g.699598T>G , LRG_488:g.699598T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3020T>G MANE Select ENSP00000373700.3:p.Phe1007Cys
ENST00000431873.6:c.186T>G
ENST00000389048.7:c.3020T>G ENSP00000373700.3:p.Phe1007Cys
ENST00000618119.4:c.1889T>G ENSP00000482733.1:p.Phe630Cys
NM_004304.4:c.3020T>G NP_004295.2:p.Phe1007Cys
XM_024452778.1:c.173T>G XP_024308546.1:p.Phe58Cys
XR_001738688.2:n.3876T>G
NM_004304.5:c.3020T>G MANE Select NP_004295.2:p.Phe1007Cys
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