Canonical Allele Identifier: CA346466056

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143395
• MyVariant Identifiers: chr2:g.29420461C>G (hg19) ; chr2:g.29197595C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197595C>G , CM000664.2:g.29197595C>G	GRCh38
NC_000002.11:g.29420461C>G , CM000664.1:g.29420461C>G	GRCh37
NC_000002.10:g.29273965C>G	NCBI36
NG_009445.1:g.728972G>C , LRG_488:g.728972G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*589C>G (CLIP4)	ENSP00000508948.1:n.*589C>G
ENST00000389048.8:c.4020G>C (ALK) MANE Select	ENSP00000373700.3:p.Glu1340Asp
ENST00000431873.6:c.1247G>C (ALK)
ENST00000638605.1:n.897G>C (ALK)
ENST00000642122.1:c.816G>C (ALK)	ENSP00000493203.1:p.Glu272Asp
ENST00000389048.7:c.4020G>C (ALK)	ENSP00000373700.3:p.Glu1340Asp
ENST00000431873.5:c.900G>C (ALK)	ENSP00000414027.2:p.Glu300Asp
ENST00000618119.4:c.2889G>C (ALK)	ENSP00000482733.1:p.Glu963Asp
NM_004304.4:c.4020G>C (ALK)	NP_004295.2:p.Glu1340Asp
NM_001353765.1:c.816G>C (ALK)	NP_001340694.1:p.Glu272Asp
XM_024452778.1:c.1173G>C (ALK)	XP_024308546.1:p.Glu391Asp
XM_024452779.1:c.816G>C (ALK)	XP_024308547.1:p.Glu272Asp
NM_004304.5:c.4020G>C (ALK) MANE Select	NP_004295.2:p.Glu1340Asp
NM_001353765.2:c.816G>C (ALK)	NP_001340694.1:p.Glu272Asp