Canonical Allele Identifier: CA1241092852

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226971G= , CM000664.2:g.29226971G=	GRCh38
NC_000002.11:g.29449837G= , CM000664.1:g.29449837G=	GRCh37
NC_000002.10:g.29303341G=	NCBI36
NG_009445.1:g.699596C= , LRG_488:g.699596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3018C= MANE Select	ENSP00000373700.3:p.Cys1006=
ENST00000431873.6:c.184C=
ENST00000389048.7:c.3018C=	ENSP00000373700.3:p.Cys1006=
ENST00000618119.4:c.1887C=	ENSP00000482733.1:p.Cys629=
NM_004304.4:c.3018C=	NP_004295.2:p.Cys1006=
XM_024452778.1:c.171C=	XP_024308546.1:p.Cys57=
XR_001738688.2:n.3874C=
NM_004304.5:c.3018C= MANE Select	NP_004295.2:p.Cys1006=