Canonical Allele Identifier: CA346474208
Gene: ALK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328391T>G , CM000664.2:g.29328391T>G GRCh38
NC_000002.11:g.29551257T>G , CM000664.1:g.29551257T>G GRCh37
NC_000002.10:g.29404761T>G NCBI36
NG_009445.1:g.598176A>C , LRG_488:g.598176A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1373A>C MANE Select ENSP00000373700.3:p.His458Pro
ENST00000389048.7:c.1373A>C ENSP00000373700.3:p.His458Pro
ENST00000618119.4:c.242A>C ENSP00000482733.1:p.His81Pro
NM_004304.4:c.1373A>C NP_004295.2:p.His458Pro
XR_939920.1:n.699T>G
XR_939921.1:n.680+5863T>G
XR_001738688.2:n.2303A>C
XR_939920.2:n.589T>G
XR_939921.2:n.576+5863T>G
NM_004304.5:c.1373A>C MANE Select NP_004295.2:p.His458Pro