Canonical Allele Identifier: CA1241075332

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197587G= , CM000664.2:g.29197587G=	GRCh38
NC_000002.11:g.29420453G= , CM000664.1:g.29420453G=	GRCh37
NC_000002.10:g.29273957G=	NCBI36
NG_009445.1:g.728980C= , LRG_488:g.728980C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*581G= (CLIP4)	ENSP00000508948.1:n.*581G=
ENST00000389048.8:c.4028C= (ALK) MANE Select	ENSP00000373700.3:p.Thr1343=
ENST00000431873.6:c.1255C= (ALK)
ENST00000638605.1:n.905C= (ALK)
ENST00000642122.1:c.824C= (ALK)	ENSP00000493203.1:p.Thr275=
ENST00000389048.7:c.4028C= (ALK)	ENSP00000373700.3:p.Thr1343=
ENST00000431873.5:c.908C= (ALK)	ENSP00000414027.2:p.Thr303=
ENST00000618119.4:c.2897C= (ALK)	ENSP00000482733.1:p.Thr966=
NM_004304.4:c.4028C= (ALK)	NP_004295.2:p.Thr1343=
NM_001353765.1:c.824C= (ALK)	NP_001340694.1:p.Thr275=
XM_024452778.1:c.1181C= (ALK)	XP_024308546.1:p.Thr394=
XM_024452779.1:c.824C= (ALK)	XP_024308547.1:p.Thr275=
NM_004304.5:c.4028C= (ALK) MANE Select	NP_004295.2:p.Thr1343=
NM_001353765.2:c.824C= (ALK)	NP_001340694.1:p.Thr275=