Canonical Allele Identifier: CA346466043

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143382
• MyVariant Identifiers: chr2:g.29420458A>T (hg19) ; chr2:g.29197592A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197592A>T , CM000664.2:g.29197592A>T	GRCh38
NC_000002.11:g.29420458A>T , CM000664.1:g.29420458A>T	GRCh37
NC_000002.10:g.29273962A>T	NCBI36
NG_009445.1:g.728975T>A , LRG_488:g.728975T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*586A>T (CLIP4)	ENSP00000508948.1:n.*586A>T
ENST00000389048.8:c.4023T>A (ALK) MANE Select	ENSP00000373700.3:p.Phe1341Leu
ENST00000431873.6:c.1250T>A (ALK)
ENST00000638605.1:n.900T>A (ALK)
ENST00000642122.1:c.819T>A (ALK)	ENSP00000493203.1:p.Phe273Leu
ENST00000389048.7:c.4023T>A (ALK)	ENSP00000373700.3:p.Phe1341Leu
ENST00000431873.5:c.903T>A (ALK)	ENSP00000414027.2:p.Phe301Leu
ENST00000618119.4:c.2892T>A (ALK)	ENSP00000482733.1:p.Phe964Leu
NM_004304.4:c.4023T>A (ALK)	NP_004295.2:p.Phe1341Leu
NM_001353765.1:c.819T>A (ALK)	NP_001340694.1:p.Phe273Leu
XM_024452778.1:c.1176T>A (ALK)	XP_024308546.1:p.Phe392Leu
XM_024452779.1:c.819T>A (ALK)	XP_024308547.1:p.Phe273Leu
NM_004304.5:c.4023T>A (ALK) MANE Select	NP_004295.2:p.Phe1341Leu
NM_001353765.2:c.819T>A (ALK)	NP_001340694.1:p.Phe273Leu