Canonical Allele Identifier: CA346467926
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29449897G>C (hg19) chr2:g.29227031G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227031G>C , CM000664.2:g.29227031G>C GRCh38
NC_000002.11:g.29449897G>C , CM000664.1:g.29449897G>C GRCh37
NC_000002.10:g.29303401G>C NCBI36
NG_009445.1:g.699536C>G , LRG_488:g.699536C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2958C>G MANE Select ENSP00000373700.3:p.Asn986Lys
ENST00000431873.6:c.124C>G
ENST00000389048.7:c.2958C>G ENSP00000373700.3:p.Asn986Lys
ENST00000618119.4:c.1827C>G ENSP00000482733.1:p.Asn609Lys
NM_004304.4:c.2958C>G NP_004295.2:p.Asn986Lys
XM_024452778.1:c.111C>G XP_024308546.1:p.Asn37Lys
XR_001738688.2:n.3814C>G
NM_004304.5:c.2958C>G MANE Select NP_004295.2:p.Asn986Lys
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