Canonical Allele Identifier: CA346466051

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143391
• MyVariant Identifiers: chr2:g.29420460A>C (hg19) ; chr2:g.29197594A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197594A>C , CM000664.2:g.29197594A>C	GRCh38
NC_000002.11:g.29420460A>C , CM000664.1:g.29420460A>C	GRCh37
NC_000002.10:g.29273964A>C	NCBI36
NG_009445.1:g.728973T>G , LRG_488:g.728973T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*588A>C (CLIP4)	ENSP00000508948.1:n.*588A>C
ENST00000389048.8:c.4021T>G (ALK) MANE Select	ENSP00000373700.3:p.Phe1341Val
ENST00000431873.6:c.1248T>G (ALK)
ENST00000638605.1:n.898T>G (ALK)
ENST00000642122.1:c.817T>G (ALK)	ENSP00000493203.1:p.Phe273Val
ENST00000389048.7:c.4021T>G (ALK)	ENSP00000373700.3:p.Phe1341Val
ENST00000431873.5:c.901T>G (ALK)	ENSP00000414027.2:p.Phe301Val
ENST00000618119.4:c.2890T>G (ALK)	ENSP00000482733.1:p.Phe964Val
NM_004304.4:c.4021T>G (ALK)	NP_004295.2:p.Phe1341Val
NM_001353765.1:c.817T>G (ALK)	NP_001340694.1:p.Phe273Val
XM_024452778.1:c.1174T>G (ALK)	XP_024308546.1:p.Phe392Val
XM_024452779.1:c.817T>G (ALK)	XP_024308547.1:p.Phe273Val
NM_004304.5:c.4021T>G (ALK) MANE Select	NP_004295.2:p.Phe1341Val
NM_001353765.2:c.817T>G (ALK)	NP_001340694.1:p.Phe273Val