Canonical Allele Identifier: CA346466020

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143368
• MyVariant Identifiers: chr2:g.29420454T>A (hg19) ; chr2:g.29197588T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197588T>A , CM000664.2:g.29197588T>A	GRCh38
NC_000002.11:g.29420454T>A , CM000664.1:g.29420454T>A	GRCh37
NC_000002.10:g.29273958T>A	NCBI36
NG_009445.1:g.728979A>T , LRG_488:g.728979A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*582T>A (CLIP4)	ENSP00000508948.1:n.*582T>A
ENST00000389048.8:c.4027A>T (ALK) MANE Select	ENSP00000373700.3:p.Thr1343Ser
ENST00000431873.6:c.1254A>T (ALK)
ENST00000638605.1:n.904A>T (ALK)
ENST00000642122.1:c.823A>T (ALK)	ENSP00000493203.1:p.Thr275Ser
ENST00000389048.7:c.4027A>T (ALK)	ENSP00000373700.3:p.Thr1343Ser
ENST00000431873.5:c.907A>T (ALK)	ENSP00000414027.2:p.Thr303Ser
ENST00000618119.4:c.2896A>T (ALK)	ENSP00000482733.1:p.Thr966Ser
NM_004304.4:c.4027A>T (ALK)	NP_004295.2:p.Thr1343Ser
NM_001353765.1:c.823A>T (ALK)	NP_001340694.1:p.Thr275Ser
XM_024452778.1:c.1180A>T (ALK)	XP_024308546.1:p.Thr394Ser
XM_024452779.1:c.823A>T (ALK)	XP_024308547.1:p.Thr275Ser
NM_004304.5:c.4027A>T (ALK) MANE Select	NP_004295.2:p.Thr1343Ser
NM_001353765.2:c.823A>T (ALK)	NP_001340694.1:p.Thr275Ser