Canonical Allele Identifier: CA346465780

Gene: CLIP4 ALK

Linked Data

• COSMIC: COSM5575864
• MyVariant Identifiers: chr2:g.29420412G>A (hg19) ; chr2:g.29197546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197546G>A , CM000664.2:g.29197546G>A	GRCh38
NC_000002.11:g.29420412G>A , CM000664.1:g.29420412G>A	GRCh37
NC_000002.10:g.29273916G>A	NCBI36
NG_009445.1:g.729021C>T , LRG_488:g.729021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*540G>A (CLIP4)	ENSP00000508948.1:n.*540G>A
ENST00000389048.8:c.4069C>T (ALK) MANE Select	ENSP00000373700.3:p.Pro1357Ser
ENST00000431873.6:c.1296C>T (ALK)
ENST00000638605.1:n.946C>T (ALK)
ENST00000642122.1:c.865C>T (ALK)	ENSP00000493203.1:p.Pro289Ser
ENST00000389048.7:c.4069C>T (ALK)	ENSP00000373700.3:p.Pro1357Ser
ENST00000431873.5:c.949C>T (ALK)	ENSP00000414027.2:p.Pro317Ser
ENST00000618119.4:c.2938C>T (ALK)	ENSP00000482733.1:p.Pro980Ser
NM_004304.4:c.4069C>T (ALK)	NP_004295.2:p.Pro1357Ser
NM_001353765.1:c.865C>T (ALK)	NP_001340694.1:p.Pro289Ser
XM_024452778.1:c.1222C>T (ALK)	XP_024308546.1:p.Pro408Ser
XM_024452779.1:c.865C>T (ALK)	XP_024308547.1:p.Pro289Ser
NM_004304.5:c.4069C>T (ALK) MANE Select	NP_004295.2:p.Pro1357Ser
NM_001353765.2:c.865C>T (ALK)	NP_001340694.1:p.Pro289Ser