Canonical Allele Identifier: CA1241144704
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328492C= , CM000664.2:g.29328492C= GRCh38
NC_000002.11:g.29551358C= , CM000664.1:g.29551358C= GRCh37
NC_000002.10:g.29404862C= NCBI36
NG_009445.1:g.598075G= , LRG_488:g.598075G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-11G= MANE Select ENSP00000373700.3:n.1283-11G=
ENST00000389048.7:c.1283-11G= ENSP00000373700.3:n.1283-11G=
ENST00000618119.4:c.152-11G= ENSP00000482733.1:n.152-11G=
NM_004304.4:c.1283-11G= NP_004295.2:n.1283-11G=
XR_939920.1:n.800C=
XR_939921.1:n.680+5964C=
XR_001738688.2:n.2213-11G=
XR_939920.2:n.690C=
XR_939921.2:n.576+5964C=
NM_004304.5:c.1283-11G= MANE Select NP_004295.2:n.1283-11G=