Canonical Allele Identifier: CA2838032959

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197539T>G , CM000664.2:g.29197539T>G	GRCh38
NC_000002.11:g.29420405T>G , CM000664.1:g.29420405T>G	GRCh37
NC_000002.10:g.29273909T>G	NCBI36
NG_009445.1:g.729028A>C , LRG_488:g.729028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*533T>G (CLIP4)	ENSP00000508948.1:n.*533T>G
ENST00000389048.8:c.4073+3A>C (ALK) MANE Select	ENSP00000373700.3:n.4073+3A>C
ENST00000431873.6:c.1300+3A>C (ALK)
ENST00000638605.1:n.950+3A>C (ALK)
ENST00000642122.1:c.869+3A>C (ALK)	ENSP00000493203.1:n.869+3A>C
ENST00000389048.7:c.4073+3A>C (ALK)	ENSP00000373700.3:n.4073+3A>C
ENST00000431873.5:c.953+3A>C (ALK)	ENSP00000414027.2:n.953+3A>C
ENST00000618119.4:c.2942+3A>C (ALK)	ENSP00000482733.1:n.2942+3A>C
NM_004304.4:c.4073+3A>C (ALK)	NP_004295.2:n.4073+3A>C
NM_001353765.1:c.869+3A>C (ALK)	NP_001340694.1:n.869+3A>C
XM_024452778.1:c.1226+3A>C (ALK)	XP_024308546.1:n.1226+3A>C
XM_024452779.1:c.869+3A>C (ALK)	XP_024308547.1:n.869+3A>C
NM_004304.5:c.4073+3A>C (ALK) MANE Select	NP_004295.2:n.4073+3A>C
NM_001353765.2:c.869+3A>C (ALK)	NP_001340694.1:n.869+3A>C