Canonical Allele Identifier: CA346466074

Gene: CLIP4 ALK

Linked Data

• MyVariant Identifiers: chr2:g.29420465A>C (hg19) ; chr2:g.29197599A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197599A>C , CM000664.2:g.29197599A>C	GRCh38
NC_000002.11:g.29420465A>C , CM000664.1:g.29420465A>C	GRCh37
NC_000002.10:g.29273969A>C	NCBI36
NG_009445.1:g.728968T>G , LRG_488:g.728968T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*593A>C (CLIP4)	ENSP00000508948.1:n.*593A>C
ENST00000389048.8:c.4016T>G (ALK) MANE Select	ENSP00000373700.3:p.Leu1339Arg
ENST00000431873.6:c.1243T>G (ALK)
ENST00000638605.1:n.893T>G (ALK)
ENST00000642122.1:c.812T>G (ALK)	ENSP00000493203.1:p.Leu271Arg
ENST00000389048.7:c.4016T>G (ALK)	ENSP00000373700.3:p.Leu1339Arg
ENST00000431873.5:c.896T>G (ALK)	ENSP00000414027.2:p.Leu299Arg
ENST00000618119.4:c.2885T>G (ALK)	ENSP00000482733.1:p.Leu962Arg
NM_004304.4:c.4016T>G (ALK)	NP_004295.2:p.Leu1339Arg
NM_001353765.1:c.812T>G (ALK)	NP_001340694.1:p.Leu271Arg
XM_024452778.1:c.1169T>G (ALK)	XP_024308546.1:p.Leu390Arg
XM_024452779.1:c.812T>G (ALK)	XP_024308547.1:p.Leu271Arg
NM_004304.5:c.4016T>G (ALK) MANE Select	NP_004295.2:p.Leu1339Arg
NM_001353765.2:c.812T>G (ALK)	NP_001340694.1:p.Leu271Arg