Canonical Allele Identifier: CA44637687

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs752290241
• MyVariant Identifiers: chr2:g.29420080_29420084del (hg19) ; chr2:g.29197214_29197218del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197216_29197220del , CM000664.2:g.29197216_29197220del	GRCh38
NC_000002.11:g.29420082_29420086del , CM000664.1:g.29420082_29420086del	GRCh37
NC_000002.10:g.29273586_29273590del	NCBI36
NG_009445.1:g.729349_729353del , LRG_488:g.729349_729353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*210_*214del (CLIP4)	ENSP00000508948.1:n.*210_*214del
ENST00000389048.8:c.4073+324_4073+328del (ALK) MANE Select	ENSP00000373700.3:n.4073+324_4073+328del
ENST00000431873.6:c.1300+324_1300+328del (ALK)
ENST00000638605.1:n.950+324_950+328del (ALK)
ENST00000642122.1:c.869+324_869+328del (ALK)	ENSP00000493203.1:n.869+324_869+328del
ENST00000389048.7:c.4073+324_4073+328del (ALK)	ENSP00000373700.3:n.4073+324_4073+328del
ENST00000431873.5:c.953+324_953+328del (ALK)	ENSP00000414027.2:n.953+324_953+328del
ENST00000618119.4:c.2942+324_2942+328del (ALK)	ENSP00000482733.1:n.2942+324_2942+328del
NM_004304.4:c.4073+324_4073+328del (ALK)	NP_004295.2:n.4073+324_4073+328del
NM_001353765.1:c.869+324_869+328del (ALK)	NP_001340694.1:n.869+324_869+328del
XM_024452778.1:c.1226+324_1226+328del (ALK)	XP_024308546.1:n.1226+324_1226+328del
XM_024452779.1:c.869+324_869+328del (ALK)	XP_024308547.1:n.869+324_869+328del
NM_004304.5:c.4073+324_4073+328del (ALK) MANE Select	NP_004295.2:n.4073+324_4073+328del
NM_001353765.2:c.869+324_869+328del (ALK)	NP_001340694.1:n.869+324_869+328del