Canonical Allele Identifier: CA346466032

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 2840075
• ClinVar RCV Id: RCV003635084
• dbSNP Id: rs2148143378
• MyVariant Identifiers: chr2:g.29420456A>T (hg19) ; chr2:g.29197590A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197590A>T , CM000664.2:g.29197590A>T	GRCh38
NC_000002.11:g.29420456A>T , CM000664.1:g.29420456A>T	GRCh37
NC_000002.10:g.29273960A>T	NCBI36
NG_009445.1:g.728977T>A , LRG_488:g.728977T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*584A>T (CLIP4)	ENSP00000508948.1:n.*584A>T
ENST00000389048.8:c.4025T>A (ALK) MANE Select	ENSP00000373700.3:p.Val1342Asp
ENST00000431873.6:c.1252T>A (ALK)
ENST00000638605.1:n.902T>A (ALK)
ENST00000642122.1:c.821T>A (ALK)	ENSP00000493203.1:p.Val274Asp
ENST00000389048.7:c.4025T>A (ALK)	ENSP00000373700.3:p.Val1342Asp
ENST00000431873.5:c.905T>A (ALK)	ENSP00000414027.2:p.Val302Asp
ENST00000618119.4:c.2894T>A (ALK)	ENSP00000482733.1:p.Val965Asp
NM_004304.4:c.4025T>A (ALK)	NP_004295.2:p.Val1342Asp
NM_001353765.1:c.821T>A (ALK)	NP_001340694.1:p.Val274Asp
XM_024452778.1:c.1178T>A (ALK)	XP_024308546.1:p.Val393Asp
XM_024452779.1:c.821T>A (ALK)	XP_024308547.1:p.Val274Asp
NM_004304.5:c.4025T>A (ALK) MANE Select	NP_004295.2:p.Val1342Asp
NM_001353765.2:c.821T>A (ALK)	NP_001340694.1:p.Val274Asp