Canonical Allele Identifier: CA346462652

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 952972
• ClinVar RCV Id: RCV001225192
• dbSNP Id: rs1307483937
• MyVariant Identifiers: chr2:g.29416635C>T (hg19) ; chr2:g.29193769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193769C>T , CM000664.2:g.29193769C>T	GRCh38
NC_000002.11:g.29416635C>T , CM000664.1:g.29416635C>T	GRCh37
NC_000002.10:g.29270139C>T	NCBI36
NG_009445.1:g.732798G>A , LRG_488:g.732798G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3159C>T (CLIP4)	ENSP00000508948.1:n.1923-3159C>T
ENST00000389048.8:c.4318G>A (ALK) MANE Select	ENSP00000373700.3:p.Ala1440Thr
ENST00000431873.6:c.1545G>A (ALK)
ENST00000638605.1:n.1195G>A (ALK)
ENST00000642122.1:c.1114G>A (ALK)	ENSP00000493203.1:p.Ala372Thr
ENST00000389048.7:c.4318G>A (ALK)	ENSP00000373700.3:p.Ala1440Thr
ENST00000431873.5:c.1198G>A (ALK)	ENSP00000414027.2:p.Ala400Thr
ENST00000618119.4:c.3187G>A (ALK)	ENSP00000482733.1:p.Ala1063Thr
NM_004304.4:c.4318G>A (ALK)	NP_004295.2:p.Ala1440Thr
NM_001353765.1:c.1114G>A (ALK)	NP_001340694.1:p.Ala372Thr
XM_024452778.1:c.1471G>A (ALK)	XP_024308546.1:p.Ala491Thr
XM_024452779.1:c.1114G>A (ALK)	XP_024308547.1:p.Ala372Thr
NM_004304.5:c.4318G>A (ALK) MANE Select	NP_004295.2:p.Ala1440Thr
NM_001353765.2:c.1114G>A (ALK)	NP_001340694.1:p.Ala372Thr