Canonical Allele Identifier: CA767497610

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs1246118387
• MyVariant Identifiers: chr2:g.29420115_29420119del (hg19) ; chr2:g.29197249_29197253del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197251_29197255del , CM000664.2:g.29197251_29197255del	GRCh38
NC_000002.11:g.29420117_29420121del , CM000664.1:g.29420117_29420121del	GRCh37
NC_000002.10:g.29273621_29273625del	NCBI36
NG_009445.1:g.729314_729318del , LRG_488:g.729314_729318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*245_*249del (CLIP4)	ENSP00000508948.1:n.*245_*249del
ENST00000389048.8:c.4073+289_4073+293del (ALK) MANE Select	ENSP00000373700.3:n.4073+289_4073+293del
ENST00000431873.6:c.1300+289_1300+293del (ALK)
ENST00000638605.1:n.950+289_950+293del (ALK)
ENST00000642122.1:c.869+289_869+293del (ALK)	ENSP00000493203.1:n.869+289_869+293del
ENST00000389048.7:c.4073+289_4073+293del (ALK)	ENSP00000373700.3:n.4073+289_4073+293del
ENST00000431873.5:c.953+289_953+293del (ALK)	ENSP00000414027.2:n.953+289_953+293del
ENST00000618119.4:c.2942+289_2942+293del (ALK)	ENSP00000482733.1:n.2942+289_2942+293del
NM_004304.4:c.4073+289_4073+293del (ALK)	NP_004295.2:n.4073+289_4073+293del
NM_001353765.1:c.869+289_869+293del (ALK)	NP_001340694.1:n.869+289_869+293del
XM_024452778.1:c.1226+289_1226+293del (ALK)	XP_024308546.1:n.1226+289_1226+293del
XM_024452779.1:c.869+289_869+293del (ALK)	XP_024308547.1:n.869+289_869+293del
NM_004304.5:c.4073+289_4073+293del (ALK) MANE Select	NP_004295.2:n.4073+289_4073+293del
NM_001353765.2:c.869+289_869+293del (ALK)	NP_001340694.1:n.869+289_869+293del