Canonical Allele Identifier: CA346466061

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 485086
• ClinVar RCV Id: RCV000570452 ; RCV000819572
• dbSNP Id: rs1469977891
• gnomAD v4: 2-29197596-T-C
• MyVariant Identifiers: chr2:g.29420462T>C (hg19) ; chr2:g.29197596T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197596T>C , CM000664.2:g.29197596T>C	GRCh38
NC_000002.11:g.29420462T>C , CM000664.1:g.29420462T>C	GRCh37
NC_000002.10:g.29273966T>C	NCBI36
NG_009445.1:g.728971A>G , LRG_488:g.728971A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*590T>C (CLIP4)	ENSP00000508948.1:n.*590T>C
ENST00000389048.8:c.4019A>G (ALK) MANE Select	ENSP00000373700.3:p.Glu1340Gly
ENST00000431873.6:c.1246A>G (ALK)
ENST00000638605.1:n.896A>G (ALK)
ENST00000642122.1:c.815A>G (ALK)	ENSP00000493203.1:p.Glu272Gly
ENST00000389048.7:c.4019A>G (ALK)	ENSP00000373700.3:p.Glu1340Gly
ENST00000431873.5:c.899A>G (ALK)	ENSP00000414027.2:p.Glu300Gly
ENST00000618119.4:c.2888A>G (ALK)	ENSP00000482733.1:p.Glu963Gly
NM_004304.4:c.4019A>G (ALK)	NP_004295.2:p.Glu1340Gly
NM_001353765.1:c.815A>G (ALK)	NP_001340694.1:p.Glu272Gly
XM_024452778.1:c.1172A>G (ALK)	XP_024308546.1:p.Glu391Gly
XM_024452779.1:c.815A>G (ALK)	XP_024308547.1:p.Glu272Gly
NM_004304.5:c.4019A>G (ALK) MANE Select	NP_004295.2:p.Glu1340Gly
NM_001353765.2:c.815A>G (ALK)	NP_001340694.1:p.Glu272Gly