Canonical Allele Identifier: CA1241092883
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227038T= , CM000664.2:g.29227038T= GRCh38
NC_000002.11:g.29449904T= , CM000664.1:g.29449904T= GRCh37
NC_000002.10:g.29303408T= NCBI36
NG_009445.1:g.699529A= , LRG_488:g.699529A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2951A= MANE Select ENSP00000373700.3:p.Tyr984=
ENST00000431873.6:c.117A=
ENST00000389048.7:c.2951A= ENSP00000373700.3:p.Tyr984=
ENST00000618119.4:c.1820A= ENSP00000482733.1:p.Tyr607=
NM_004304.4:c.2951A= NP_004295.2:p.Tyr984=
XM_024452778.1:c.104A= XP_024308546.1:p.Tyr35=
XR_001738688.2:n.3807A=
NM_004304.5:c.2951A= MANE Select NP_004295.2:p.Tyr984=