Canonical Allele Identifier: CA1241075052

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197429_29197431delinsAGG , CM000664.2:g.29197429_29197431delinsAGG	GRCh38
NC_000002.11:g.29420295_29420297delinsAGG , CM000664.1:g.29420295_29420297delinsAGG	GRCh37
NC_000002.10:g.29273799_29273801delinsAGG	NCBI36
NG_009445.1:g.729136_729138delinsCCT , LRG_488:g.729136_729138delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*423_*425delinsAGG (CLIP4)	ENSP00000508948.1:n.*423_*425delinsAGG
ENST00000389048.8:c.4073+111_4073+113delinsCCT (ALK) MANE Select	ENSP00000373700.3:n.4073+111_4073+113delinsCCT
ENST00000431873.6:c.1300+111_1300+113delinsCCT (ALK)
ENST00000638605.1:n.950+111_950+113delinsCCT (ALK)
ENST00000642122.1:c.869+111_869+113delinsCCT (ALK)	ENSP00000493203.1:n.869+111_869+113delinsCCT
ENST00000389048.7:c.4073+111_4073+113delinsCCT (ALK)	ENSP00000373700.3:n.4073+111_4073+113delinsCCT
ENST00000431873.5:c.953+111_953+113delinsCCT (ALK)	ENSP00000414027.2:n.953+111_953+113delinsCCT
ENST00000618119.4:c.2942+111_2942+113delinsCCT (ALK)	ENSP00000482733.1:n.2942+111_2942+113delinsCCT
NM_004304.4:c.4073+111_4073+113delinsCCT (ALK)	NP_004295.2:n.4073+111_4073+113delinsCCT
NM_001353765.1:c.869+111_869+113delinsCCT (ALK)	NP_001340694.1:n.869+111_869+113delinsCCT
XM_024452778.1:c.1226+111_1226+113delinsCCT (ALK)	XP_024308546.1:n.1226+111_1226+113delinsCCT
XM_024452779.1:c.869+111_869+113delinsCCT (ALK)	XP_024308547.1:n.869+111_869+113delinsCCT
NM_004304.5:c.4073+111_4073+113delinsCCT (ALK) MANE Select	NP_004295.2:n.4073+111_4073+113delinsCCT
NM_001353765.2:c.869+111_869+113delinsCCT (ALK)	NP_001340694.1:n.869+111_869+113delinsCCT