Canonical Allele Identifier: CA346466053

Gene: CLIP4 ALK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*588A>G (CLIP4)	ENSP00000508948.1:n.*588A>G
ENST00000389048.8:c.4021T>C (ALK) MANE Select	ENSP00000373700.3:p.Phe1341Leu
ENST00000431873.6:c.1248T>C (ALK)
ENST00000638605.1:n.898T>C (ALK)
ENST00000642122.1:c.817T>C (ALK)	ENSP00000493203.1:p.Phe273Leu
ENST00000389048.7:c.4021T>C (ALK)	ENSP00000373700.3:p.Phe1341Leu
ENST00000431873.5:c.901T>C (ALK)	ENSP00000414027.2:p.Phe301Leu
ENST00000618119.4:c.2890T>C (ALK)	ENSP00000482733.1:p.Phe964Leu
NM_004304.4:c.4021T>C (ALK)	NP_004295.2:p.Phe1341Leu
NM_001353765.1:c.817T>C (ALK)	NP_001340694.1:p.Phe273Leu
XM_024452778.1:c.1174T>C (ALK)	XP_024308546.1:p.Phe392Leu
XM_024452779.1:c.817T>C (ALK)	XP_024308547.1:p.Phe273Leu
NM_004304.5:c.4021T>C (ALK) MANE Select	NP_004295.2:p.Phe1341Leu
NM_001353765.2:c.817T>C (ALK)	NP_001340694.1:p.Phe273Leu