Canonical Allele Identifier: CA425433903

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143357
• gnomAD v4: 2-29197586-G-T
• MyVariant Identifiers: chr2:g.29420452G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197586G>T , CM000664.2:g.29197586G>T	GRCh38
NC_000002.11:g.29420452G>T , CM000664.1:g.29420452G>T	GRCh37
NC_000002.10:g.29273956G>T	NCBI36
NG_009445.1:g.728981C>A , LRG_488:g.728981C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689605.1:c.*580G>T (CLIP4)	ENSP00000508948.1:n.*580G>T
ENST00000389048.8:c.4029C>A (ALK) MANE Select	ENSP00000373700.3:p.Thr1343=
ENST00000431873.6:c.1256C>A (ALK)
ENST00000638605.1:n.906C>A (ALK)
ENST00000642122.1:c.825C>A (ALK)	ENSP00000493203.1:p.Thr275=
ENST00000389048.7:c.4029C>A (ALK)	ENSP00000373700.3:p.Thr1343=
ENST00000431873.5:c.909C>A (ALK)	ENSP00000414027.2:p.Thr303=
ENST00000618119.4:c.2898C>A (ALK)	ENSP00000482733.1:p.Thr966=
NM_004304.4:c.4029C>A (ALK)	NP_004295.2:p.Thr1343=
NM_001353765.1:c.825C>A (ALK)	NP_001340694.1:p.Thr275=
XM_024452778.1:c.1182C>A (ALK)	XP_024308546.1:p.Thr394=
XM_024452779.1:c.825C>A (ALK)	XP_024308547.1:p.Thr275=
NM_004304.5:c.4029C>A (ALK) MANE Select	NP_004295.2:p.Thr1343=
NM_001353765.2:c.825C>A (ALK)	NP_001340694.1:p.Thr275=