Canonical Allele Identifier: CA1241092850

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226969A= , CM000664.2:g.29226969A=	GRCh38
NC_000002.11:g.29449835A= , CM000664.1:g.29449835A=	GRCh37
NC_000002.10:g.29303339A=	NCBI36
NG_009445.1:g.699598T= , LRG_488:g.699598T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3020T= MANE Select	ENSP00000373700.3:p.Phe1007=
ENST00000431873.6:c.186T=
ENST00000389048.7:c.3020T=	ENSP00000373700.3:p.Phe1007=
ENST00000618119.4:c.1889T=	ENSP00000482733.1:p.Phe630=
NM_004304.4:c.3020T=	NP_004295.2:p.Phe1007=
XM_024452778.1:c.173T=	XP_024308546.1:p.Phe58=
XR_001738688.2:n.3876T=
NM_004304.5:c.3020T= MANE Select	NP_004295.2:p.Phe1007=