Canonical Allele Identifier: CA10581961

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 239831
• ClinVar RCV Id: RCV000230663 ; RCV002372276
• dbSNP Id: rs540427775
• gnomAD v3: 2-29197631-C-T
• gnomAD v4: 2-29197631-C-T
• MyVariant Identifiers: chr2:g.29420497C>T (hg19) ; chr2:g.29197631C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197631C>T , CM000664.2:g.29197631C>T	GRCh38
NC_000002.11:g.29420497C>T , CM000664.1:g.29420497C>T	GRCh37
NC_000002.10:g.29274001C>T	NCBI36
NG_009445.1:g.728936G>A , LRG_488:g.728936G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*625C>T (CLIP4)	ENSP00000508948.1:n.*625C>T
ENST00000389048.8:c.3984G>A (ALK) MANE Select	ENSP00000373700.3:p.Met1328Ile
ENST00000431873.6:c.1211G>A (ALK)
ENST00000638605.1:n.861G>A (ALK)
ENST00000642122.1:c.780G>A (ALK)	ENSP00000493203.1:p.Met260Ile
ENST00000389048.7:c.3984G>A (ALK)	ENSP00000373700.3:p.Met1328Ile
ENST00000431873.5:c.864G>A (ALK)	ENSP00000414027.2:p.Met288Ile
ENST00000618119.4:c.2853G>A (ALK)	ENSP00000482733.1:p.Met951Ile
NM_004304.4:c.3984G>A (ALK)	NP_004295.2:p.Met1328Ile
NM_001353765.1:c.780G>A (ALK)	NP_001340694.1:p.Met260Ile
XM_024452778.1:c.1137G>A (ALK)	XP_024308546.1:p.Met379Ile
XM_024452779.1:c.780G>A (ALK)	XP_024308547.1:p.Met260Ile
NM_004304.5:c.3984G>A (ALK) MANE Select	NP_004295.2:p.Met1328Ile
NM_001353765.2:c.780G>A (ALK)	NP_001340694.1:p.Met260Ile