Canonical Allele Identifier: CA531766851

Gene: ALK

Linked Data

• dbSNP Id: rs1558621772
• gnomAD v2: 2-29443610-C-CT
• gnomAD v4: 2-29220744-C-CT
• MyVariant Identifiers: chr2:g.29443610_29443611insT (hg19) ; chr2:g.29220744_29220745insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220745dup , CM000664.2:g.29220745dup	GRCh38
NC_000002.11:g.29443611dup , CM000664.1:g.29443611dup	GRCh37
NC_000002.10:g.29297115dup	NCBI36
NG_009445.1:g.705822dup , LRG_488:g.705822dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3606dup MANE Select	ENSP00000373700.3:p.Asp1203ArgfsTer?
ENST00000431873.6:c.833dup
ENST00000638605.1:n.483dup
ENST00000642122.1:c.402dup	ENSP00000493203.1:p.Asp135ArgfsTer?
ENST00000389048.7:c.3606dup	ENSP00000373700.3:p.Asp1203ArgfsTer?
ENST00000431873.5:c.486dup	ENSP00000414027.2:p.Asp163ArgfsTer?
ENST00000618119.4:c.2475dup	ENSP00000482733.1:p.Asp826ArgfsTer?
NM_004304.4:c.3606dup	NP_004295.2:p.Asp1203ArgfsTer?
NM_001353765.1:c.402dup	NP_001340694.1:p.Asp135ArgfsTer?
XM_024452778.1:c.759dup	XP_024308546.1:p.Asp254ArgfsTer?
XM_024452779.1:c.402dup	XP_024308547.1:p.Asp135ArgfsTer?
NM_004304.5:c.3606dup MANE Select	NP_004295.2:p.Asp1203ArgfsTer?
NM_001353765.2:c.402dup	NP_001340694.1:p.Asp135ArgfsTer?