Canonical Allele Identifier: CA346466246

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 957636
• ClinVar RCV Id: RCV001230644
• dbSNP Id: rs1669057104
• MyVariant Identifiers: chr2:g.29420493A>G (hg19) ; chr2:g.29197627A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197627A>G , CM000664.2:g.29197627A>G	GRCh38
NC_000002.11:g.29420493A>G , CM000664.1:g.29420493A>G	GRCh37
NC_000002.10:g.29273997A>G	NCBI36
NG_009445.1:g.728940T>C , LRG_488:g.728940T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*621A>G (CLIP4)	ENSP00000508948.1:n.*621A>G
ENST00000389048.8:c.3988T>C (ALK) MANE Select	ENSP00000373700.3:p.Tyr1330His
ENST00000431873.6:c.1215T>C (ALK)
ENST00000638605.1:n.865T>C (ALK)
ENST00000642122.1:c.784T>C (ALK)	ENSP00000493203.1:p.Tyr262His
ENST00000389048.7:c.3988T>C (ALK)	ENSP00000373700.3:p.Tyr1330His
ENST00000431873.5:c.868T>C (ALK)	ENSP00000414027.2:p.Tyr290His
ENST00000618119.4:c.2857T>C (ALK)	ENSP00000482733.1:p.Tyr953His
NM_004304.4:c.3988T>C (ALK)	NP_004295.2:p.Tyr1330His
NM_001353765.1:c.784T>C (ALK)	NP_001340694.1:p.Tyr262His
XM_024452778.1:c.1141T>C (ALK)	XP_024308546.1:p.Tyr381His
XM_024452779.1:c.784T>C (ALK)	XP_024308547.1:p.Tyr262His
NM_004304.5:c.3988T>C (ALK) MANE Select	NP_004295.2:p.Tyr1330His
NM_001353765.2:c.784T>C (ALK)	NP_001340694.1:p.Tyr262His