Canonical Allele Identifier: CA1241071332

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193749G= , CM000664.2:g.29193749G=	GRCh38
NC_000002.11:g.29416615G= , CM000664.1:g.29416615G=	GRCh37
NC_000002.10:g.29270119G=	NCBI36
NG_009445.1:g.732818C= , LRG_488:g.732818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3179G= (CLIP4)	ENSP00000508948.1:n.1923-3179G=
ENST00000389048.8:c.4338C= (ALK) MANE Select	ENSP00000373700.3:p.Thr1446=
ENST00000431873.6:c.1565C= (ALK)
ENST00000638605.1:n.1215C= (ALK)
ENST00000642122.1:c.1134C= (ALK)	ENSP00000493203.1:p.Thr378=
ENST00000389048.7:c.4338C= (ALK)	ENSP00000373700.3:p.Thr1446=
ENST00000431873.5:c.1218C= (ALK)	ENSP00000414027.2:p.Thr406=
ENST00000618119.4:c.3207C= (ALK)	ENSP00000482733.1:p.Thr1069=
NM_004304.4:c.4338C= (ALK)	NP_004295.2:p.Thr1446=
NM_001353765.1:c.1134C= (ALK)	NP_001340694.1:p.Thr378=
XM_024452778.1:c.1491C= (ALK)	XP_024308546.1:p.Thr497=
XM_024452779.1:c.1134C= (ALK)	XP_024308547.1:p.Thr378=
NM_004304.5:c.4338C= (ALK) MANE Select	NP_004295.2:p.Thr1446=
NM_001353765.2:c.1134C= (ALK)	NP_001340694.1:p.Thr378=