Canonical Allele Identifier: CA2658458239

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs771308439
• gnomAD v4: 2-29197687-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197687G>A , CM000664.2:g.29197687G>A	GRCh38
NC_000002.11:g.29420553G>A , CM000664.1:g.29420553G>A	GRCh37
NC_000002.10:g.29274057G>A	NCBI36
NG_009445.1:g.728880C>T , LRG_488:g.728880C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*681G>A (CLIP4)	ENSP00000508948.1:n.*681G>A
ENST00000389048.8:c.3939-11C>T (ALK) MANE Select	ENSP00000373700.3:n.3939-11C>T
ENST00000431873.6:c.1166-11C>T (ALK)
ENST00000638605.1:n.816-11C>T (ALK)
ENST00000642122.1:c.735-11C>T (ALK)	ENSP00000493203.1:n.735-11C>T
ENST00000389048.7:c.3939-11C>T (ALK)	ENSP00000373700.3:n.3939-11C>T
ENST00000431873.5:c.819-11C>T (ALK)	ENSP00000414027.2:n.819-11C>T
ENST00000618119.4:c.2808-11C>T (ALK)	ENSP00000482733.1:n.2808-11C>T
NM_004304.4:c.3939-11C>T (ALK)	NP_004295.2:n.3939-11C>T
NM_001353765.1:c.735-11C>T (ALK)	NP_001340694.1:n.735-11C>T
XM_024452778.1:c.1092-11C>T (ALK)	XP_024308546.1:n.1092-11C>T
XM_024452779.1:c.735-11C>T (ALK)	XP_024308547.1:n.735-11C>T
NM_004304.5:c.3939-11C>T (ALK) MANE Select	NP_004295.2:n.3939-11C>T
NM_001353765.2:c.735-11C>T (ALK)	NP_001340694.1:n.735-11C>T