Canonical Allele Identifier: CA767497834

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs1167839959
• MyVariant Identifiers: chr2:g.29420429_29420430insC (hg19) ; chr2:g.29197563_29197564insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197563_29197564insC , CM000664.2:g.29197563_29197564insC	GRCh38
NC_000002.11:g.29420429_29420430insC , CM000664.1:g.29420429_29420430insC	GRCh37
NC_000002.10:g.29273933_29273934insC	NCBI36
NG_009445.1:g.729003_729004insG , LRG_488:g.729003_729004insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*557_*558insC (CLIP4)	ENSP00000508948.1:n.*557_*558insC
ENST00000389048.8:c.4051_4052insG (ALK) MANE Select	ENSP00000373700.3:p.Pro1351ArgfsTer21
ENST00000431873.6:c.1278_1279insG (ALK)
ENST00000638605.1:n.928_929insG (ALK)
ENST00000642122.1:c.847_848insG (ALK)	ENSP00000493203.1:p.Pro283ArgfsTer21
ENST00000389048.7:c.4051_4052insG (ALK)	ENSP00000373700.3:p.Pro1351ArgfsTer21
ENST00000431873.5:c.931_932insG (ALK)	ENSP00000414027.2:p.Pro311ArgfsTer21
ENST00000618119.4:c.2920_2921insG (ALK)	ENSP00000482733.1:p.Pro974ArgfsTer21
NM_004304.4:c.4051_4052insG (ALK)	NP_004295.2:p.Pro1351ArgfsTer21
NM_001353765.1:c.847_848insG (ALK)	NP_001340694.1:p.Pro283ArgfsTer21
XM_024452778.1:c.1204_1205insG (ALK)	XP_024308546.1:p.Pro402ArgfsTer21
XM_024452779.1:c.847_848insG (ALK)	XP_024308547.1:p.Pro283ArgfsTer21
NM_004304.5:c.4051_4052insG (ALK) MANE Select	NP_004295.2:p.Pro1351ArgfsTer21
NM_001353765.2:c.847_848insG (ALK)	NP_001340694.1:p.Pro283ArgfsTer21