Canonical Allele Identifier: CA346466048

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143387
• MyVariant Identifiers: chr2:g.29420459A>T (hg19) ; chr2:g.29197593A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197593A>T , CM000664.2:g.29197593A>T	GRCh38
NC_000002.11:g.29420459A>T , CM000664.1:g.29420459A>T	GRCh37
NC_000002.10:g.29273963A>T	NCBI36
NG_009445.1:g.728974T>A , LRG_488:g.728974T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*587A>T (CLIP4)	ENSP00000508948.1:n.*587A>T
ENST00000389048.8:c.4022T>A (ALK) MANE Select	ENSP00000373700.3:p.Phe1341Tyr
ENST00000431873.6:c.1249T>A (ALK)
ENST00000638605.1:n.899T>A (ALK)
ENST00000642122.1:c.818T>A (ALK)	ENSP00000493203.1:p.Phe273Tyr
ENST00000389048.7:c.4022T>A (ALK)	ENSP00000373700.3:p.Phe1341Tyr
ENST00000431873.5:c.902T>A (ALK)	ENSP00000414027.2:p.Phe301Tyr
ENST00000618119.4:c.2891T>A (ALK)	ENSP00000482733.1:p.Phe964Tyr
NM_004304.4:c.4022T>A (ALK)	NP_004295.2:p.Phe1341Tyr
NM_001353765.1:c.818T>A (ALK)	NP_001340694.1:p.Phe273Tyr
XM_024452778.1:c.1175T>A (ALK)	XP_024308546.1:p.Phe392Tyr
XM_024452779.1:c.818T>A (ALK)	XP_024308547.1:p.Phe273Tyr
NM_004304.5:c.4022T>A (ALK) MANE Select	NP_004295.2:p.Phe1341Tyr
NM_001353765.2:c.818T>A (ALK)	NP_001340694.1:p.Phe273Tyr