Canonical Allele Identifier: CA1241071257

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193713A= , CM000664.2:g.29193713A=	GRCh38
NC_000002.11:g.29416579A= , CM000664.1:g.29416579A=	GRCh37
NC_000002.10:g.29270083A=	NCBI36
NG_009445.1:g.732854T= , LRG_488:g.732854T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3215A= (CLIP4)	ENSP00000508948.1:n.1923-3215A=
ENST00000389048.8:c.4374T= (ALK) MANE Select	ENSP00000373700.3:p.Ala1458=
ENST00000431873.6:c.1601T= (ALK)
ENST00000638605.1:n.1251T= (ALK)
ENST00000642122.1:c.1170T= (ALK)	ENSP00000493203.1:p.Ala390=
ENST00000389048.7:c.4374T= (ALK)	ENSP00000373700.3:p.Ala1458=
ENST00000431873.5:c.1254T= (ALK)	ENSP00000414027.2:p.Ala418=
ENST00000618119.4:c.3243T= (ALK)	ENSP00000482733.1:p.Ala1081=
NM_004304.4:c.4374T= (ALK)	NP_004295.2:p.Ala1458=
NM_001353765.1:c.1170T= (ALK)	NP_001340694.1:p.Ala390=
XM_024452778.1:c.1527T= (ALK)	XP_024308546.1:p.Ala509=
XM_024452779.1:c.1170T= (ALK)	XP_024308547.1:p.Ala390=
NM_004304.5:c.4374T= (ALK) MANE Select	NP_004295.2:p.Ala1458=
NM_001353765.2:c.1170T= (ALK)	NP_001340694.1:p.Ala390=