Canonical Allele Identifier: CA425619160

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs1256422825
• MyVariant Identifiers: chr2:g.29416549C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193683C>G , CM000664.2:g.29193683C>G	GRCh38
NC_000002.11:g.29416549C>G , CM000664.1:g.29416549C>G	GRCh37
NC_000002.10:g.29270053C>G	NCBI36
NG_009445.1:g.732884G>C , LRG_488:g.732884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3245C>G (CLIP4)	ENSP00000508948.1:n.1923-3245C>G
ENST00000389048.8:c.4404G>C (ALK) MANE Select	ENSP00000373700.3:p.Gly1468=
ENST00000431873.6:c.1631G>C (ALK)
ENST00000638605.1:n.1281G>C (ALK)
ENST00000642122.1:c.1200G>C (ALK)	ENSP00000493203.1:p.Gly400=
ENST00000389048.7:c.4404G>C (ALK)	ENSP00000373700.3:p.Gly1468=
ENST00000431873.5:c.1284G>C (ALK)	ENSP00000414027.2:p.Gly428=
ENST00000618119.4:c.3273G>C (ALK)	ENSP00000482733.1:p.Gly1091=
NM_004304.4:c.4404G>C (ALK)	NP_004295.2:p.Gly1468=
NM_001353765.1:c.1200G>C (ALK)	NP_001340694.1:p.Gly400=
XM_024452778.1:c.1557G>C (ALK)	XP_024308546.1:p.Gly519=
XM_024452779.1:c.1200G>C (ALK)	XP_024308547.1:p.Gly400=
NM_004304.5:c.4404G>C (ALK) MANE Select	NP_004295.2:p.Gly1468=
NM_001353765.2:c.1200G>C (ALK)	NP_001340694.1:p.Gly400=