Canonical Allele Identifier: CA1241089802

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220821T= , CM000664.2:g.29220821T=	GRCh38
NC_000002.11:g.29443687T= , CM000664.1:g.29443687T=	GRCh37
NC_000002.10:g.29297191T=	NCBI36
NG_009445.1:g.705746A= , LRG_488:g.705746A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3530A= MANE Select	ENSP00000373700.3:p.Gln1177=
ENST00000431873.6:c.757A=
ENST00000638605.1:n.407A=
ENST00000642122.1:c.326A=	ENSP00000493203.1:p.Gln109=
ENST00000389048.7:c.3530A=	ENSP00000373700.3:p.Gln1177=
ENST00000431873.5:c.410A=	ENSP00000414027.2:p.Gln137=
ENST00000618119.4:c.2399A=	ENSP00000482733.1:p.Gln800=
NM_004304.4:c.3530A=	NP_004295.2:p.Gln1177=
NM_001353765.1:c.326A=	NP_001340694.1:p.Gln109=
XM_024452778.1:c.683A=	XP_024308546.1:p.Gln228=
XM_024452779.1:c.326A=	XP_024308547.1:p.Gln109=
NM_004304.5:c.3530A= MANE Select	NP_004295.2:p.Gln1177=
NM_001353765.2:c.326A=	NP_001340694.1:p.Gln109=