Canonical Allele Identifier: CA425433908

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 2700221
• ClinVar RCV Id: RCV003517949
• MyVariant Identifiers: chr2:g.29420458A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197592A>G , CM000664.2:g.29197592A>G	GRCh38
NC_000002.11:g.29420458A>G , CM000664.1:g.29420458A>G	GRCh37
NC_000002.10:g.29273962A>G	NCBI36
NG_009445.1:g.728975T>C , LRG_488:g.728975T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*586A>G (CLIP4)	ENSP00000508948.1:n.*586A>G
ENST00000389048.8:c.4023T>C (ALK) MANE Select	ENSP00000373700.3:p.Phe1341=
ENST00000431873.6:c.1250T>C (ALK)
ENST00000638605.1:n.900T>C (ALK)
ENST00000642122.1:c.819T>C (ALK)	ENSP00000493203.1:p.Phe273=
ENST00000389048.7:c.4023T>C (ALK)	ENSP00000373700.3:p.Phe1341=
ENST00000431873.5:c.903T>C (ALK)	ENSP00000414027.2:p.Phe301=
ENST00000618119.4:c.2892T>C (ALK)	ENSP00000482733.1:p.Phe964=
NM_004304.4:c.4023T>C (ALK)	NP_004295.2:p.Phe1341=
NM_001353765.1:c.819T>C (ALK)	NP_001340694.1:p.Phe273=
XM_024452778.1:c.1176T>C (ALK)	XP_024308546.1:p.Phe392=
XM_024452779.1:c.819T>C (ALK)	XP_024308547.1:p.Phe273=
NM_004304.5:c.4023T>C (ALK) MANE Select	NP_004295.2:p.Phe1341=
NM_001353765.2:c.819T>C (ALK)	NP_001340694.1:p.Phe273=