Canonical Allele Identifier: CA425618761

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193225C>T , CM000664.2:g.29193225C>T	GRCh38
NC_000002.11:g.29416091C>T , CM000664.1:g.29416091C>T	GRCh37
NC_000002.10:g.29269595C>T	NCBI36
NG_009445.1:g.733342G>A , LRG_488:g.733342G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3703C>T (CLIP4)	ENSP00000508948.1:n.1923-3703C>T
ENST00000389048.8:c.4862G>A (ALK) MANE Select	ENSP00000373700.3:p.Ter1621=
ENST00000431873.6:c.2089G>A (ALK)
ENST00000638605.1:n.1739G>A (ALK)
ENST00000642122.1:c.1658G>A (ALK)	ENSP00000493203.1:p.Ter553=
ENST00000389048.7:c.4862G>A (ALK)	ENSP00000373700.3:p.Ter1621=
ENST00000431873.5:c.1742G>A (ALK)	ENSP00000414027.2:p.Ter581=
ENST00000618119.4:c.3731G>A (ALK)	ENSP00000482733.1:p.Ter1244=
NM_004304.4:c.4862G>A (ALK)	NP_004295.2:p.Ter1621=
NM_001353765.1:c.1658G>A (ALK)	NP_001340694.1:p.Ter553=
XM_024452778.1:c.2015G>A (ALK)	XP_024308546.1:p.Ter672=
XM_024452779.1:c.1658G>A (ALK)	XP_024308547.1:p.Ter553=
NM_004304.5:c.4862G>A (ALK) MANE Select	NP_004295.2:p.Ter1621=
NM_001353765.2:c.1658G>A (ALK)	NP_001340694.1:p.Ter553=