Canonical Allele Identifier: CA2573134633

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1474455
• ClinVar RCV Id: RCV001971281
• dbSNP Id: rs2148143702

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197686G>C , CM000664.2:g.29197686G>C	GRCh38
NC_000002.11:g.29420552G>C , CM000664.1:g.29420552G>C	GRCh37
NC_000002.10:g.29274056G>C	NCBI36
NG_009445.1:g.728881C>G , LRG_488:g.728881C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*680G>C (CLIP4)	ENSP00000508948.1:n.*680G>C
ENST00000389048.8:c.3939-10C>G (ALK) MANE Select	ENSP00000373700.3:n.3939-10C>G
ENST00000431873.6:c.1166-10C>G (ALK)
ENST00000638605.1:n.816-10C>G (ALK)
ENST00000642122.1:c.735-10C>G (ALK)	ENSP00000493203.1:n.735-10C>G
ENST00000389048.7:c.3939-10C>G (ALK)	ENSP00000373700.3:n.3939-10C>G
ENST00000431873.5:c.819-10C>G (ALK)	ENSP00000414027.2:n.819-10C>G
ENST00000618119.4:c.2808-10C>G (ALK)	ENSP00000482733.1:n.2808-10C>G
NM_004304.4:c.3939-10C>G (ALK)	NP_004295.2:n.3939-10C>G
NM_001353765.1:c.735-10C>G (ALK)	NP_001340694.1:n.735-10C>G
XM_024452778.1:c.1092-10C>G (ALK)	XP_024308546.1:n.1092-10C>G
XM_024452779.1:c.735-10C>G (ALK)	XP_024308547.1:n.735-10C>G
NM_004304.5:c.3939-10C>G (ALK) MANE Select	NP_004295.2:n.3939-10C>G
NM_001353765.2:c.735-10C>G (ALK)	NP_001340694.1:n.735-10C>G