Canonical Allele Identifier: CA1241071311

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193743_29193756delinsGGAGGTGGTAGGCA , CM000664.2:g.29193743_29193756delinsGGAGGTGGTAGGCA	GRCh38
NC_000002.11:g.29416609_29416622delinsGGAGGTGGTAGGCA , CM000664.1:g.29416609_29416622delinsGGAGGTGGTAGGCA	GRCh37
NC_000002.10:g.29270113_29270126delinsGGAGGTGGTAGGCA	NCBI36
NG_009445.1:g.732811_732824delinsTGCCTACCACCTCC , LRG_488:g.732811_732824delinsTGCCTACCACCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3185_1923-3172delinsGGAGGTGGTAGGCA (CLIP4)	ENSP00000508948.1:n.1923-3185_1923-3172delinsGGAGGTGGTAGGCA
ENST00000389048.8:c.4331_4344delinsTGCCTACCACCTCC (ALK) MANE Select	ENSP00000373700.3:p.Leu1444=
ENST00000431873.6:c.1558_1571delinsTGCCTACCACCTCC (ALK)
ENST00000638605.1:n.1208_1221delinsTGCCTACCACCTCC (ALK)
ENST00000642122.1:c.1127_1140delinsTGCCTACCACCTCC (ALK)	ENSP00000493203.1:p.Leu376=
ENST00000389048.7:c.4331_4344delinsTGCCTACCACCTCC (ALK)	ENSP00000373700.3:p.Leu1444=
ENST00000431873.5:c.1211_1224delinsTGCCTACCACCTCC (ALK)	ENSP00000414027.2:p.Leu404=
ENST00000618119.4:c.3200_3213delinsTGCCTACCACCTCC (ALK)	ENSP00000482733.1:p.Leu1067=
NM_004304.4:c.4331_4344delinsTGCCTACCACCTCC (ALK)	NP_004295.2:p.Leu1444=
NM_001353765.1:c.1127_1140delinsTGCCTACCACCTCC (ALK)	NP_001340694.1:p.Leu376=
XM_024452778.1:c.1484_1497delinsTGCCTACCACCTCC (ALK)	XP_024308546.1:p.Leu495=
XM_024452779.1:c.1127_1140delinsTGCCTACCACCTCC (ALK)	XP_024308547.1:p.Leu376=
NM_004304.5:c.4331_4344delinsTGCCTACCACCTCC (ALK) MANE Select	NP_004295.2:p.Leu1444=
NM_001353765.2:c.1127_1140delinsTGCCTACCACCTCC (ALK)	NP_001340694.1:p.Leu376=