Canonical Allele Identifier: CA1241144719
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328510G= , CM000664.2:g.29328510G= GRCh38
NC_000002.11:g.29551376G= , CM000664.1:g.29551376G= GRCh37
NC_000002.10:g.29404880G= NCBI36
NG_009445.1:g.598057C= , LRG_488:g.598057C=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-29C= MANE Select ENSP00000373700.3:n.1283-29C=
ENST00000389048.7:c.1283-29C= ENSP00000373700.3:n.1283-29C=
ENST00000618119.4:c.152-29C= ENSP00000482733.1:n.152-29C=
NM_004304.4:c.1283-29C= NP_004295.2:n.1283-29C=
XR_939920.1:n.817+1G=
XR_939921.1:n.680+5982G=
XR_001738688.2:n.2213-29C=
XR_939920.2:n.707+1G=
XR_939921.2:n.576+5982G=
NM_004304.5:c.1283-29C= MANE Select NP_004295.2:n.1283-29C=