Canonical Allele Identifier: CA1241075335

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197596T= , CM000664.2:g.29197596T=	GRCh38
NC_000002.11:g.29420462T= , CM000664.1:g.29420462T=	GRCh37
NC_000002.10:g.29273966T=	NCBI36
NG_009445.1:g.728971A= , LRG_488:g.728971A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*590T= (CLIP4)	ENSP00000508948.1:n.*590T=
ENST00000389048.8:c.4019A= (ALK) MANE Select	ENSP00000373700.3:p.Glu1340=
ENST00000431873.6:c.1246A= (ALK)
ENST00000638605.1:n.896A= (ALK)
ENST00000642122.1:c.815A= (ALK)	ENSP00000493203.1:p.Glu272=
ENST00000389048.7:c.4019A= (ALK)	ENSP00000373700.3:p.Glu1340=
ENST00000431873.5:c.899A= (ALK)	ENSP00000414027.2:p.Glu300=
ENST00000618119.4:c.2888A= (ALK)	ENSP00000482733.1:p.Glu963=
NM_004304.4:c.4019A= (ALK)	NP_004295.2:p.Glu1340=
NM_001353765.1:c.815A= (ALK)	NP_001340694.1:p.Glu272=
XM_024452778.1:c.1172A= (ALK)	XP_024308546.1:p.Glu391=
XM_024452779.1:c.815A= (ALK)	XP_024308547.1:p.Glu272=
NM_004304.5:c.4019A= (ALK) MANE Select	NP_004295.2:p.Glu1340=
NM_001353765.2:c.815A= (ALK)	NP_001340694.1:p.Glu272=