Canonical Allele Identifier: CA1241090442

Gene: ALK

Linked Data

• dbSNP Id: rs1669821813
• gnomAD v4: 2-29222227-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222230_29222231del , CM000664.2:g.29222230_29222231del	GRCh38
NC_000002.11:g.29445096_29445097del , CM000664.1:g.29445096_29445097del	GRCh37
NC_000002.10:g.29298600_29298601del	NCBI36
NG_009445.1:g.704338_704339del , LRG_488:g.704338_704339del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+115_3515+116del MANE Select	ENSP00000373700.3:n.3515+115_3515+116del
ENST00000431873.6:c.742+115_742+116del
ENST00000638605.1:n.392+115_392+116del
ENST00000642122.1:c.311+115_311+116del	ENSP00000493203.1:n.311+115_311+116del
ENST00000389048.7:c.3515+115_3515+116del	ENSP00000373700.3:n.3515+115_3515+116del
ENST00000431873.5:c.395+115_395+116del	ENSP00000414027.2:n.395+115_395+116del
ENST00000453137.1:c.209+115_209+116del	ENSP00000387488.1:n.209+115_209+116del
ENST00000618119.4:c.2384+115_2384+116del	ENSP00000482733.1:n.2384+115_2384+116del
NM_004304.4:c.3515+115_3515+116del	NP_004295.2:n.3515+115_3515+116del
NM_001353765.1:c.311+115_311+116del	NP_001340694.1:n.311+115_311+116del
XM_024452778.1:c.668+115_668+116del	XP_024308546.1:n.668+115_668+116del
XM_024452779.1:c.311+115_311+116del	XP_024308547.1:n.311+115_311+116del
NM_004304.5:c.3515+115_3515+116del MANE Select	NP_004295.2:n.3515+115_3515+116del
NM_001353765.2:c.311+115_311+116del	NP_001340694.1:n.311+115_311+116del