Canonical Allele Identifier: CA44637138

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29196607A>G , CM000664.2:g.29196607A>G	GRCh38
NC_000002.11:g.29419473A>G , CM000664.1:g.29419473A>G	GRCh37
NC_000002.10:g.29272977A>G	NCBI36
NG_009445.1:g.729960T>C , LRG_488:g.729960T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4164+163T>C (ALK) MANE Select	NP_004295.2:n.4164+163T>C
ENST00000389048.8:c.4164+163T>C (ALK) MANE Select	ENSP00000373700.3:n.4164+163T>C
NM_001353765.1:c.960+163T>C (ALK)	NP_001340694.1:n.960+163T>C
NM_001353765.2:c.960+163T>C (ALK)	NP_001340694.1:n.960+163T>C
NM_004304.4:c.4164+163T>C (ALK)	NP_004295.2:n.4164+163T>C
ENST00000389048.7:c.4164+163T>C (ALK)	ENSP00000373700.3:n.4164+163T>C
ENST00000431873.5:c.1044+163T>C (ALK)	ENSP00000414027.2:n.1044+163T>C
ENST00000431873.6:c.1391+163T>C (ALK)
ENST00000618119.4:c.3033+163T>C (ALK)	ENSP00000482733.1:n.3033+163T>C
ENST00000638605.1:n.1041+163T>C (ALK)
ENST00000642122.1:c.960+163T>C (ALK)	ENSP00000493203.1:n.960+163T>C
ENST00000689605.1:c.1923-321A>G (CLIP4)	ENSP00000508948.1:n.1923-321A>G
XM_024452778.1:c.1317+163T>C (ALK)	XP_024308546.1:n.1317+163T>C
XM_024452779.1:c.960+163T>C (ALK)	XP_024308547.1:n.960+163T>C