Canonical Allele Identifier: CA1241075099

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197467A= , CM000664.2:g.29197467A=	GRCh38
NC_000002.11:g.29420333A= , CM000664.1:g.29420333A=	GRCh37
NC_000002.10:g.29273837A=	NCBI36
NG_009445.1:g.729100T= , LRG_488:g.729100T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*461A= (CLIP4)	ENSP00000508948.1:n.*461A=
ENST00000389048.8:c.4073+75T= (ALK) MANE Select	ENSP00000373700.3:n.4073+75T=
ENST00000431873.6:c.1300+75T= (ALK)
ENST00000638605.1:n.950+75T= (ALK)
ENST00000642122.1:c.869+75T= (ALK)	ENSP00000493203.1:n.869+75T=
ENST00000389048.7:c.4073+75T= (ALK)	ENSP00000373700.3:n.4073+75T=
ENST00000431873.5:c.953+75T= (ALK)	ENSP00000414027.2:n.953+75T=
ENST00000618119.4:c.2942+75T= (ALK)	ENSP00000482733.1:n.2942+75T=
NM_004304.4:c.4073+75T= (ALK)	NP_004295.2:n.4073+75T=
NM_001353765.1:c.869+75T= (ALK)	NP_001340694.1:n.869+75T=
XM_024452778.1:c.1226+75T= (ALK)	XP_024308546.1:n.1226+75T=
XM_024452779.1:c.869+75T= (ALK)	XP_024308547.1:n.869+75T=
NM_004304.5:c.4073+75T= (ALK) MANE Select	NP_004295.2:n.4073+75T=
NM_001353765.2:c.869+75T= (ALK)	NP_001340694.1:n.869+75T=