Canonical Allele Identifier: CA1241074830

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs1669044231

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197198A>C , CM000664.2:g.29197198A>C	GRCh38
NC_000002.11:g.29420064A>C , CM000664.1:g.29420064A>C	GRCh37
NC_000002.10:g.29273568A>C	NCBI36
NG_009445.1:g.729369T>G , LRG_488:g.729369T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*192A>C (CLIP4)	ENSP00000508948.1:n.*192A>C
ENST00000389048.8:c.4074-338T>G (ALK) MANE Select	ENSP00000373700.3:n.4074-338T>G
ENST00000431873.6:c.1301-338T>G (ALK)
ENST00000638605.1:n.951-338T>G (ALK)
ENST00000642122.1:c.870-338T>G (ALK)	ENSP00000493203.1:n.870-338T>G
ENST00000389048.7:c.4074-338T>G (ALK)	ENSP00000373700.3:n.4074-338T>G
ENST00000431873.5:c.954-338T>G (ALK)	ENSP00000414027.2:n.954-338T>G
ENST00000618119.4:c.2943-338T>G (ALK)	ENSP00000482733.1:n.2943-338T>G
NM_004304.4:c.4074-338T>G (ALK)	NP_004295.2:n.4074-338T>G
NM_001353765.1:c.870-338T>G (ALK)	NP_001340694.1:n.870-338T>G
XM_024452778.1:c.1227-338T>G (ALK)	XP_024308546.1:n.1227-338T>G
XM_024452779.1:c.870-338T>G (ALK)	XP_024308547.1:n.870-338T>G
NM_004304.5:c.4074-338T>G (ALK) MANE Select	NP_004295.2:n.4074-338T>G
NM_001353765.2:c.870-338T>G (ALK)	NP_001340694.1:n.870-338T>G