Canonical Allele Identifier: CA1241075338

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197598C= , CM000664.2:g.29197598C=	GRCh38
NC_000002.11:g.29420464C= , CM000664.1:g.29420464C=	GRCh37
NC_000002.10:g.29273968C=	NCBI36
NG_009445.1:g.728969G= , LRG_488:g.728969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*592C= (CLIP4)	ENSP00000508948.1:n.*592C=
ENST00000389048.8:c.4017G= (ALK) MANE Select	ENSP00000373700.3:p.Leu1339=
ENST00000431873.6:c.1244G= (ALK)
ENST00000638605.1:n.894G= (ALK)
ENST00000642122.1:c.813G= (ALK)	ENSP00000493203.1:p.Leu271=
ENST00000389048.7:c.4017G= (ALK)	ENSP00000373700.3:p.Leu1339=
ENST00000431873.5:c.897G= (ALK)	ENSP00000414027.2:p.Leu299=
ENST00000618119.4:c.2886G= (ALK)	ENSP00000482733.1:p.Leu962=
NM_004304.4:c.4017G= (ALK)	NP_004295.2:p.Leu1339=
NM_001353765.1:c.813G= (ALK)	NP_001340694.1:p.Leu271=
XM_024452778.1:c.1170G= (ALK)	XP_024308546.1:p.Leu390=
XM_024452779.1:c.813G= (ALK)	XP_024308547.1:p.Leu271=
NM_004304.5:c.4017G= (ALK) MANE Select	NP_004295.2:p.Leu1339=
NM_001353765.2:c.813G= (ALK)	NP_001340694.1:p.Leu271=