Canonical Allele Identifier: CA2658458169

Gene: ALK

Linked Data

• gnomAD v4: 2-29222196-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222198_29222199del , CM000664.2:g.29222198_29222199del	GRCh38
NC_000002.11:g.29445064_29445065del , CM000664.1:g.29445064_29445065del	GRCh37
NC_000002.10:g.29298568_29298569del	NCBI36
NG_009445.1:g.704369_704370del , LRG_488:g.704369_704370del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+146_3515+147del MANE Select	ENSP00000373700.3:n.3515+146_3515+147del
ENST00000431873.6:c.742+146_742+147del
ENST00000638605.1:n.392+146_392+147del
ENST00000642122.1:c.311+146_311+147del	ENSP00000493203.1:n.311+146_311+147del
ENST00000389048.7:c.3515+146_3515+147del	ENSP00000373700.3:n.3515+146_3515+147del
ENST00000431873.5:c.395+146_395+147del	ENSP00000414027.2:n.395+146_395+147del
ENST00000453137.1:c.209+146_209+147del	ENSP00000387488.1:n.209+146_209+147del
ENST00000618119.4:c.2384+146_2384+147del	ENSP00000482733.1:n.2384+146_2384+147del
NM_004304.4:c.3515+146_3515+147del	NP_004295.2:n.3515+146_3515+147del
NM_001353765.1:c.311+146_311+147del	NP_001340694.1:n.311+146_311+147del
XM_024452778.1:c.668+146_668+147del	XP_024308546.1:n.668+146_668+147del
XM_024452779.1:c.311+146_311+147del	XP_024308547.1:n.311+146_311+147del
NM_004304.5:c.3515+146_3515+147del MANE Select	NP_004295.2:n.3515+146_3515+147del
NM_001353765.2:c.311+146_311+147del	NP_001340694.1:n.311+146_311+147del