Canonical Allele Identifier: CA1241090522

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222378C= , CM000664.2:g.29222378C=	GRCh38
NC_000002.11:g.29445244C= , CM000664.1:g.29445244C=	GRCh37
NC_000002.10:g.29298748C=	NCBI36
NG_009445.1:g.704189G= , LRG_488:g.704189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3481G= MANE Select	ENSP00000373700.3:p.Glu1161=
ENST00000431873.6:c.708G=
ENST00000638605.1:n.358G=
ENST00000642122.1:c.277G=	ENSP00000493203.1:p.Glu93=
ENST00000389048.7:c.3481G=	ENSP00000373700.3:p.Glu1161=
ENST00000431873.5:c.361G=	ENSP00000414027.2:p.Glu121=
ENST00000453137.1:c.175G=	ENSP00000387488.1:p.Glu59=
ENST00000618119.4:c.2350G=	ENSP00000482733.1:p.Glu784=
NM_004304.4:c.3481G=	NP_004295.2:p.Glu1161=
NM_001353765.1:c.277G=	NP_001340694.1:p.Glu93=
XM_024452778.1:c.634G=	XP_024308546.1:p.Glu212=
XM_024452779.1:c.277G=	XP_024308547.1:p.Glu93=
NM_004304.5:c.3481G= MANE Select	NP_004295.2:p.Glu1161=
NM_001353765.2:c.277G=	NP_001340694.1:p.Glu93=