Canonical Allele Identifier: CA2658458292

Gene: CLIP4 ALK

Linked Data

• gnomAD v4: 2-29197750-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197750C>A , CM000664.2:g.29197750C>A	GRCh38
NC_000002.11:g.29420616C>A , CM000664.1:g.29420616C>A	GRCh37
NC_000002.10:g.29274120C>A	NCBI36
NG_009445.1:g.728817G>T , LRG_488:g.728817G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*744C>A (CLIP4)	ENSP00000508948.1:n.*744C>A
ENST00000389048.8:c.3939-74G>T (ALK) MANE Select	ENSP00000373700.3:n.3939-74G>T
ENST00000431873.6:c.1166-74G>T (ALK)
ENST00000638605.1:n.816-74G>T (ALK)
ENST00000642122.1:c.735-74G>T (ALK)	ENSP00000493203.1:n.735-74G>T
ENST00000389048.7:c.3939-74G>T (ALK)	ENSP00000373700.3:n.3939-74G>T
ENST00000431873.5:c.819-74G>T (ALK)	ENSP00000414027.2:n.819-74G>T
ENST00000618119.4:c.2808-74G>T (ALK)	ENSP00000482733.1:n.2808-74G>T
NM_004304.4:c.3939-74G>T (ALK)	NP_004295.2:n.3939-74G>T
NM_001353765.1:c.735-74G>T (ALK)	NP_001340694.1:n.735-74G>T
XM_024452778.1:c.1092-74G>T (ALK)	XP_024308546.1:n.1092-74G>T
XM_024452779.1:c.735-74G>T (ALK)	XP_024308547.1:n.735-74G>T
NM_004304.5:c.3939-74G>T (ALK) MANE Select	NP_004295.2:n.3939-74G>T
NM_001353765.2:c.735-74G>T (ALK)	NP_001340694.1:n.735-74G>T