Canonical Allele Identifier: CA346474218
Gene: ALK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328394A>C , CM000664.2:g.29328394A>C GRCh38
NC_000002.11:g.29551260A>C , CM000664.1:g.29551260A>C GRCh37
NC_000002.10:g.29404764A>C NCBI36
NG_009445.1:g.598173T>G , LRG_488:g.598173T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1370T>G MANE Select ENSP00000373700.3:p.Phe457Cys
ENST00000389048.7:c.1370T>G ENSP00000373700.3:p.Phe457Cys
ENST00000618119.4:c.239T>G ENSP00000482733.1:p.Phe80Cys
NM_004304.4:c.1370T>G NP_004295.2:p.Phe457Cys
XR_939920.1:n.702A>C
XR_939921.1:n.680+5866A>C
XR_001738688.2:n.2300T>G
XR_939920.2:n.592A>C
XR_939921.2:n.576+5866A>C
NM_004304.5:c.1370T>G MANE Select NP_004295.2:p.Phe457Cys