Canonical Allele Identifier: CA346463350

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1525214
• ClinVar RCV Id: RCV002032286
• dbSNP Id: rs143647372
• MyVariant Identifiers: chr2:g.29416753T>A (hg19) ; chr2:g.29193887T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193887T>A , CM000664.2:g.29193887T>A	GRCh38
NC_000002.11:g.29416753T>A , CM000664.1:g.29416753T>A	GRCh37
NC_000002.10:g.29270257T>A	NCBI36
NG_009445.1:g.732680A>T , LRG_488:g.732680A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3041T>A (CLIP4)	ENSP00000508948.1:n.1923-3041T>A
ENST00000389048.8:c.4200A>T (ALK) MANE Select	ENSP00000373700.3:p.Glu1400Asp
ENST00000431873.6:c.1427A>T (ALK)
ENST00000638605.1:n.1077A>T (ALK)
ENST00000642122.1:c.996A>T (ALK)	ENSP00000493203.1:p.Glu332Asp
ENST00000389048.7:c.4200A>T (ALK)	ENSP00000373700.3:p.Glu1400Asp
ENST00000431873.5:c.1080A>T (ALK)	ENSP00000414027.2:p.Glu360Asp
ENST00000618119.4:c.3069A>T (ALK)	ENSP00000482733.1:p.Glu1023Asp
NM_004304.4:c.4200A>T (ALK)	NP_004295.2:p.Glu1400Asp
NM_001353765.1:c.996A>T (ALK)	NP_001340694.1:p.Glu332Asp
XM_024452778.1:c.1353A>T (ALK)	XP_024308546.1:p.Glu451Asp
XM_024452779.1:c.996A>T (ALK)	XP_024308547.1:p.Glu332Asp
NM_004304.5:c.4200A>T (ALK) MANE Select	NP_004295.2:p.Glu1400Asp
NM_001353765.2:c.996A>T (ALK)	NP_001340694.1:p.Glu332Asp