Canonical Allele Identifier: CA531469190

Gene: ALK

Linked Data

• dbSNP Id: rs1442079394
• gnomAD v2: 2-29445020-GAAAC-G
• gnomAD v3: 2-29222154-GAAAC-G
• gnomAD v4: 2-29222154-GAAAC-G
• MyVariant Identifiers: chr2:g.29445021_29445024del (hg19) ; chr2:g.29222155_29222158del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222157_29222160del , CM000664.2:g.29222157_29222160del	GRCh38
NC_000002.11:g.29445023_29445026del , CM000664.1:g.29445023_29445026del	GRCh37
NC_000002.10:g.29298527_29298530del	NCBI36
NG_009445.1:g.704409_704412del , LRG_488:g.704409_704412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+186_3515+189del MANE Select	ENSP00000373700.3:n.3515+186_3515+189del
ENST00000431873.6:c.742+186_742+189del
ENST00000638605.1:n.392+186_392+189del
ENST00000642122.1:c.311+186_311+189del	ENSP00000493203.1:n.311+186_311+189del
ENST00000389048.7:c.3515+186_3515+189del	ENSP00000373700.3:n.3515+186_3515+189del
ENST00000431873.5:c.395+186_395+189del	ENSP00000414027.2:n.395+186_395+189del
ENST00000453137.1:c.209+186_209+189del	ENSP00000387488.1:n.209+186_209+189del
ENST00000618119.4:c.2384+186_2384+189del	ENSP00000482733.1:n.2384+186_2384+189del
NM_004304.4:c.3515+186_3515+189del	NP_004295.2:n.3515+186_3515+189del
NM_001353765.1:c.311+186_311+189del	NP_001340694.1:n.311+186_311+189del
XM_024452778.1:c.668+186_668+189del	XP_024308546.1:n.668+186_668+189del
XM_024452779.1:c.311+186_311+189del	XP_024308547.1:n.311+186_311+189del
NM_004304.5:c.3515+186_3515+189del MANE Select	NP_004295.2:n.3515+186_3515+189del
NM_001353765.2:c.311+186_311+189del	NP_001340694.1:n.311+186_311+189del