Canonical Allele Identifier: CA2573134529

Gene: ALK

Linked Data

• ClinVar Variation Id: 1409456
• ClinVar RCV Id: RCV001913693
• dbSNP Id: rs2148166666

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220815dup , CM000664.2:g.29220815dup	GRCh38
NC_000002.11:g.29443681dup , CM000664.1:g.29443681dup	GRCh37
NC_000002.10:g.29297185dup	NCBI36
NG_009445.1:g.705753dup , LRG_488:g.705753dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3537dup MANE Select	ENSP00000373700.3:p.Val1180CysfsTer?
ENST00000431873.6:c.764dup
ENST00000638605.1:n.414dup
ENST00000642122.1:c.333dup	ENSP00000493203.1:p.Val112CysfsTer?
ENST00000389048.7:c.3537dup	ENSP00000373700.3:p.Val1180CysfsTer?
ENST00000431873.5:c.417dup	ENSP00000414027.2:p.Val140CysfsTer?
ENST00000618119.4:c.2406dup	ENSP00000482733.1:p.Val803CysfsTer?
NM_004304.4:c.3537dup	NP_004295.2:p.Val1180CysfsTer?
NM_001353765.1:c.333dup	NP_001340694.1:p.Val112CysfsTer?
XM_024452778.1:c.690dup	XP_024308546.1:p.Val231CysfsTer?
XM_024452779.1:c.333dup	XP_024308547.1:p.Val112CysfsTer?
NM_004304.5:c.3537dup MANE Select	NP_004295.2:p.Val1180CysfsTer?
NM_001353765.2:c.333dup	NP_001340694.1:p.Val112CysfsTer?