Canonical Allele Identifier: CA425433904

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1602752
• ClinVar RCV Id: RCV002141564
• dbSNP Id: rs2148143357
• MyVariant Identifiers: chr2:g.29420452G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197586G>C , CM000664.2:g.29197586G>C	GRCh38
NC_000002.11:g.29420452G>C , CM000664.1:g.29420452G>C	GRCh37
NC_000002.10:g.29273956G>C	NCBI36
NG_009445.1:g.728981C>G , LRG_488:g.728981C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*580G>C (CLIP4)	ENSP00000508948.1:n.*580G>C
ENST00000389048.8:c.4029C>G (ALK) MANE Select	ENSP00000373700.3:p.Thr1343=
ENST00000431873.6:c.1256C>G (ALK)
ENST00000638605.1:n.906C>G (ALK)
ENST00000642122.1:c.825C>G (ALK)	ENSP00000493203.1:p.Thr275=
ENST00000389048.7:c.4029C>G (ALK)	ENSP00000373700.3:p.Thr1343=
ENST00000431873.5:c.909C>G (ALK)	ENSP00000414027.2:p.Thr303=
ENST00000618119.4:c.2898C>G (ALK)	ENSP00000482733.1:p.Thr966=
NM_004304.4:c.4029C>G (ALK)	NP_004295.2:p.Thr1343=
NM_001353765.1:c.825C>G (ALK)	NP_001340694.1:p.Thr275=
XM_024452778.1:c.1182C>G (ALK)	XP_024308546.1:p.Thr394=
XM_024452779.1:c.825C>G (ALK)	XP_024308547.1:p.Thr275=
NM_004304.5:c.4029C>G (ALK) MANE Select	NP_004295.2:p.Thr1343=
NM_001353765.2:c.825C>G (ALK)	NP_001340694.1:p.Thr275=