Canonical Allele Identifier: CA2580066451

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1737122
• ClinVar RCV Id: RCV002375735

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197593_29197594del , CM000664.2:g.29197593_29197594del	GRCh38
NC_000002.11:g.29420459_29420460del , CM000664.1:g.29420459_29420460del	GRCh37
NC_000002.10:g.29273963_29273964del	NCBI36
NG_009445.1:g.728974_728975del , LRG_488:g.728974_728975del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*587_*588del (CLIP4)	ENSP00000508948.1:n.*587_*588del
ENST00000389048.8:c.4022_4023del (ALK) MANE Select	ENSP00000373700.3:p.Phe1341CysfsTer30
ENST00000431873.6:c.1249_1250del (ALK)
ENST00000638605.1:n.899_900del (ALK)
ENST00000642122.1:c.818_819del (ALK)	ENSP00000493203.1:p.Phe273CysfsTer30
ENST00000389048.7:c.4022_4023del (ALK)	ENSP00000373700.3:p.Phe1341CysfsTer30
ENST00000431873.5:c.902_903del (ALK)	ENSP00000414027.2:p.Phe301CysfsTer30
ENST00000618119.4:c.2891_2892del (ALK)	ENSP00000482733.1:p.Phe964CysfsTer30
NM_004304.4:c.4022_4023del (ALK)	NP_004295.2:p.Phe1341CysfsTer30
NM_001353765.1:c.818_819del (ALK)	NP_001340694.1:p.Phe273CysfsTer30
XM_024452778.1:c.1175_1176del (ALK)	XP_024308546.1:p.Phe392CysfsTer30
XM_024452779.1:c.818_819del (ALK)	XP_024308547.1:p.Phe273CysfsTer30
NM_004304.5:c.4022_4023del (ALK) MANE Select	NP_004295.2:p.Phe1341CysfsTer30
NM_001353765.2:c.818_819del (ALK)	NP_001340694.1:p.Phe273CysfsTer30