Canonical Allele Identifier: CA346459991

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193226A>G , CM000664.2:g.29193226A>G	GRCh38
NC_000002.11:g.29416092A>G , CM000664.1:g.29416092A>G	GRCh37
NC_000002.10:g.29269596A>G	NCBI36
NG_009445.1:g.733341T>C , LRG_488:g.733341T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3702A>G (CLIP4)	ENSP00000508948.1:n.1923-3702A>G
ENST00000389048.8:c.4861T>C (ALK) MANE Select	ENSP00000373700.3:p.Ter1621Arg
ENST00000431873.6:c.2088T>C (ALK)
ENST00000638605.1:n.1738T>C (ALK)
ENST00000642122.1:c.1657T>C (ALK)	ENSP00000493203.1:p.Ter553Arg
ENST00000389048.7:c.4861T>C (ALK)	ENSP00000373700.3:p.Ter1621Arg
ENST00000431873.5:c.1741T>C (ALK)	ENSP00000414027.2:p.Ter581Arg
ENST00000618119.4:c.3730T>C (ALK)	ENSP00000482733.1:p.Ter1244Arg
NM_004304.4:c.4861T>C (ALK)	NP_004295.2:p.Ter1621Arg
NM_001353765.1:c.1657T>C (ALK)	NP_001340694.1:p.Ter553Arg
XM_024452778.1:c.2014T>C (ALK)	XP_024308546.1:p.Ter672Arg
XM_024452779.1:c.1657T>C (ALK)	XP_024308547.1:p.Ter553Arg
NM_004304.5:c.4861T>C (ALK) MANE Select	NP_004295.2:p.Ter1621Arg
NM_001353765.2:c.1657T>C (ALK)	NP_001340694.1:p.Ter553Arg