Canonical Allele Identifier: CA425433905

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1105365
• ClinVar RCV Id: RCV001429739
• dbSNP Id: rs2148143373
• MyVariant Identifiers: chr2:g.29420455G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197589G>A , CM000664.2:g.29197589G>A	GRCh38
NC_000002.11:g.29420455G>A , CM000664.1:g.29420455G>A	GRCh37
NC_000002.10:g.29273959G>A	NCBI36
NG_009445.1:g.728978C>T , LRG_488:g.728978C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*583G>A (CLIP4)	ENSP00000508948.1:n.*583G>A
ENST00000389048.8:c.4026C>T (ALK) MANE Select	ENSP00000373700.3:p.Val1342=
ENST00000431873.6:c.1253C>T (ALK)
ENST00000638605.1:n.903C>T (ALK)
ENST00000642122.1:c.822C>T (ALK)	ENSP00000493203.1:p.Val274=
ENST00000389048.7:c.4026C>T (ALK)	ENSP00000373700.3:p.Val1342=
ENST00000431873.5:c.906C>T (ALK)	ENSP00000414027.2:p.Val302=
ENST00000618119.4:c.2895C>T (ALK)	ENSP00000482733.1:p.Val965=
NM_004304.4:c.4026C>T (ALK)	NP_004295.2:p.Val1342=
NM_001353765.1:c.822C>T (ALK)	NP_001340694.1:p.Val274=
XM_024452778.1:c.1179C>T (ALK)	XP_024308546.1:p.Val393=
XM_024452779.1:c.822C>T (ALK)	XP_024308547.1:p.Val274=
NM_004304.5:c.4026C>T (ALK) MANE Select	NP_004295.2:p.Val1342=
NM_001353765.2:c.822C>T (ALK)	NP_001340694.1:p.Val274=