Canonical Allele Identifier: CA1241089789

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220788T= , CM000664.2:g.29220788T=	GRCh38
NC_000002.11:g.29443654T= , CM000664.1:g.29443654T=	GRCh37
NC_000002.10:g.29297158T=	NCBI36
NG_009445.1:g.705779A= , LRG_488:g.705779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3563A= MANE Select	ENSP00000373700.3:p.Gln1188=
ENST00000431873.6:c.790A=
ENST00000638605.1:n.440A=
ENST00000642122.1:c.359A=	ENSP00000493203.1:p.Gln120=
ENST00000389048.7:c.3563A=	ENSP00000373700.3:p.Gln1188=
ENST00000431873.5:c.443A=	ENSP00000414027.2:p.Gln148=
ENST00000618119.4:c.2432A=	ENSP00000482733.1:p.Gln811=
NM_004304.4:c.3563A=	NP_004295.2:p.Gln1188=
NM_001353765.1:c.359A=	NP_001340694.1:p.Gln120=
XM_024452778.1:c.716A=	XP_024308546.1:p.Gln239=
XM_024452779.1:c.359A=	XP_024308547.1:p.Gln120=
NM_004304.5:c.3563A= MANE Select	NP_004295.2:p.Gln1188=
NM_001353765.2:c.359A=	NP_001340694.1:p.Gln120=