Canonical Allele Identifier: CA2698947292

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148142898

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197449_29197450insT , CM000664.2:g.29197449_29197450insT	GRCh38
NC_000002.11:g.29420315_29420316insT , CM000664.1:g.29420315_29420316insT	GRCh37
NC_000002.10:g.29273819_29273820insT	NCBI36
NG_009445.1:g.729117_729118insA , LRG_488:g.729117_729118insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*443_*444insT (CLIP4)	ENSP00000508948.1:n.*443_*444insT
ENST00000389048.8:c.4073+92_4073+93insA (ALK) MANE Select	ENSP00000373700.3:n.4073+92_4073+93insA
ENST00000431873.6:c.1300+92_1300+93insA (ALK)
ENST00000638605.1:n.950+92_950+93insA (ALK)
ENST00000642122.1:c.869+92_869+93insA (ALK)	ENSP00000493203.1:n.869+92_869+93insA
ENST00000389048.7:c.4073+92_4073+93insA (ALK)	ENSP00000373700.3:n.4073+92_4073+93insA
ENST00000431873.5:c.953+92_953+93insA (ALK)	ENSP00000414027.2:n.953+92_953+93insA
ENST00000618119.4:c.2942+92_2942+93insA (ALK)	ENSP00000482733.1:n.2942+92_2942+93insA
NM_004304.4:c.4073+92_4073+93insA (ALK)	NP_004295.2:n.4073+92_4073+93insA
NM_001353765.1:c.869+92_869+93insA (ALK)	NP_001340694.1:n.869+92_869+93insA
XM_024452778.1:c.1226+92_1226+93insA (ALK)	XP_024308546.1:n.1226+92_1226+93insA
XM_024452779.1:c.869+92_869+93insA (ALK)	XP_024308547.1:n.869+92_869+93insA
NM_004304.5:c.4073+92_4073+93insA (ALK) MANE Select	NP_004295.2:n.4073+92_4073+93insA
NM_001353765.2:c.869+92_869+93insA (ALK)	NP_001340694.1:n.869+92_869+93insA