Canonical Allele Identifier: CA1241092892

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227074A= , CM000664.2:g.29227074A=	GRCh38
NC_000002.11:g.29449940A= , CM000664.1:g.29449940A=	GRCh37
NC_000002.10:g.29303444A=	NCBI36
NG_009445.1:g.699493T= , LRG_488:g.699493T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2915T= MANE Select	ENSP00000373700.3:p.Val972=
ENST00000431873.6:c.81T=
ENST00000389048.7:c.2915T=	ENSP00000373700.3:p.Val972=
ENST00000618119.4:c.1784T=	ENSP00000482733.1:p.Val595=
NM_004304.4:c.2915T=	NP_004295.2:p.Val972=
XM_024452778.1:c.68T=	XP_024308546.1:p.Val23=
XR_001738688.2:n.3771T=
NM_004304.5:c.2915T= MANE Select	NP_004295.2:p.Val972=