Canonical Allele Identifier: CA1241092855

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226976T= , CM000664.2:g.29226976T=	GRCh38
NC_000002.11:g.29449842T= , CM000664.1:g.29449842T=	GRCh37
NC_000002.10:g.29303346T=	NCBI36
NG_009445.1:g.699591A= , LRG_488:g.699591A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3013A= MANE Select	ENSP00000373700.3:p.Ile1005=
ENST00000431873.6:c.179A=
ENST00000389048.7:c.3013A=	ENSP00000373700.3:p.Ile1005=
ENST00000618119.4:c.1882A=	ENSP00000482733.1:p.Ile628=
NM_004304.4:c.3013A=	NP_004295.2:p.Ile1005=
XM_024452778.1:c.166A=	XP_024308546.1:p.Ile56=
XR_001738688.2:n.3869A=
NM_004304.5:c.3013A= MANE Select	NP_004295.2:p.Ile1005=