Canonical Allele Identifier: CA1241089805

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220829G= , CM000664.2:g.29220829G=	GRCh38
NC_000002.11:g.29443695G= , CM000664.1:g.29443695G=	GRCh37
NC_000002.10:g.29297199G=	NCBI36
NG_009445.1:g.705738C= , LRG_488:g.705738C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3522C= MANE Select	ENSP00000373700.3:p.Phe1174=
ENST00000431873.6:c.749C=
ENST00000638605.1:n.399C=
ENST00000642122.1:c.318C=	ENSP00000493203.1:p.Phe106=
ENST00000389048.7:c.3522C=	ENSP00000373700.3:p.Phe1174=
ENST00000431873.5:c.402C=	ENSP00000414027.2:p.Phe134=
ENST00000618119.4:c.2391C=	ENSP00000482733.1:p.Phe797=
NM_004304.4:c.3522C=	NP_004295.2:p.Phe1174=
NM_001353765.1:c.318C=	NP_001340694.1:p.Phe106=
XM_024452778.1:c.675C=	XP_024308546.1:p.Phe225=
XM_024452779.1:c.318C=	XP_024308547.1:p.Phe106=
NM_004304.5:c.3522C= MANE Select	NP_004295.2:p.Phe1174=
NM_001353765.2:c.318C=	NP_001340694.1:p.Phe106=