Canonical Allele Identifier: CA346466011

Gene: CLIP4 ALK

Linked Data

• MyVariant Identifiers: chr2:g.29420451T>G (hg19) ; chr2:g.29197585T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197585T>G , CM000664.2:g.29197585T>G	GRCh38
NC_000002.11:g.29420451T>G , CM000664.1:g.29420451T>G	GRCh37
NC_000002.10:g.29273955T>G	NCBI36
NG_009445.1:g.728982A>C , LRG_488:g.728982A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*579T>G (CLIP4)	ENSP00000508948.1:n.*579T>G
ENST00000389048.8:c.4030A>C (ALK) MANE Select	ENSP00000373700.3:p.Ser1344Arg
ENST00000431873.6:c.1257A>C (ALK)
ENST00000638605.1:n.907A>C (ALK)
ENST00000642122.1:c.826A>C (ALK)	ENSP00000493203.1:p.Ser276Arg
ENST00000389048.7:c.4030A>C (ALK)	ENSP00000373700.3:p.Ser1344Arg
ENST00000431873.5:c.910A>C (ALK)	ENSP00000414027.2:p.Ser304Arg
ENST00000618119.4:c.2899A>C (ALK)	ENSP00000482733.1:p.Ser967Arg
NM_004304.4:c.4030A>C (ALK)	NP_004295.2:p.Ser1344Arg
NM_001353765.1:c.826A>C (ALK)	NP_001340694.1:p.Ser276Arg
XM_024452778.1:c.1183A>C (ALK)	XP_024308546.1:p.Ser395Arg
XM_024452779.1:c.826A>C (ALK)	XP_024308547.1:p.Ser276Arg
NM_004304.5:c.4030A>C (ALK) MANE Select	NP_004295.2:p.Ser1344Arg
NM_001353765.2:c.826A>C (ALK)	NP_001340694.1:p.Ser276Arg