Canonical Allele Identifier: CA1241071297

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193739C= , CM000664.2:g.29193739C=	GRCh38
NC_000002.11:g.29416605C= , CM000664.1:g.29416605C=	GRCh37
NC_000002.10:g.29270109C=	NCBI36
NG_009445.1:g.732828G= , LRG_488:g.732828G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3189C= (CLIP4)	ENSP00000508948.1:n.1923-3189C=
ENST00000389048.8:c.4348G= (ALK) MANE Select	ENSP00000373700.3:p.Gly1450=
ENST00000431873.6:c.1575G= (ALK)
ENST00000638605.1:n.1225G= (ALK)
ENST00000642122.1:c.1144G= (ALK)	ENSP00000493203.1:p.Gly382=
ENST00000389048.7:c.4348G= (ALK)	ENSP00000373700.3:p.Gly1450=
ENST00000431873.5:c.1228G= (ALK)	ENSP00000414027.2:p.Gly410=
ENST00000618119.4:c.3217G= (ALK)	ENSP00000482733.1:p.Gly1073=
NM_004304.4:c.4348G= (ALK)	NP_004295.2:p.Gly1450=
NM_001353765.1:c.1144G= (ALK)	NP_001340694.1:p.Gly382=
XM_024452778.1:c.1501G= (ALK)	XP_024308546.1:p.Gly501=
XM_024452779.1:c.1144G= (ALK)	XP_024308547.1:p.Gly382=
NM_004304.5:c.4348G= (ALK) MANE Select	NP_004295.2:p.Gly1450=
NM_001353765.2:c.1144G= (ALK)	NP_001340694.1:p.Gly382=