Canonical Allele Identifier: CA1241144532
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328388T= , CM000664.2:g.29328388T= GRCh38
NC_000002.11:g.29551254T= , CM000664.1:g.29551254T= GRCh37
NC_000002.10:g.29404758T= NCBI36
NG_009445.1:g.598179A= , LRG_488:g.598179A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1376A= MANE Select ENSP00000373700.3:p.Gln459=
ENST00000389048.7:c.1376A= ENSP00000373700.3:p.Gln459=
ENST00000618119.4:c.245A= ENSP00000482733.1:p.Gln82=
NM_004304.4:c.1376A= NP_004295.2:p.Gln459=
XR_939920.1:n.696T=
XR_939921.1:n.680+5860T=
XR_001738688.2:n.2306A=
XR_939920.2:n.586T=
XR_939921.2:n.576+5860T=
NM_004304.5:c.1376A= MANE Select NP_004295.2:p.Gln459=