Canonical Allele Identifier: CA1241090441

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222227_29222229delinsAGG , CM000664.2:g.29222227_29222229delinsAGG	GRCh38
NC_000002.11:g.29445093_29445095delinsAGG , CM000664.1:g.29445093_29445095delinsAGG	GRCh37
NC_000002.10:g.29298597_29298599delinsAGG	NCBI36
NG_009445.1:g.704338_704340delinsCCT , LRG_488:g.704338_704340delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+115_3515+117delinsCCT MANE Select	ENSP00000373700.3:n.3515+115_3515+117delinsCCT
ENST00000431873.6:c.742+115_742+117delinsCCT
ENST00000638605.1:n.392+115_392+117delinsCCT
ENST00000642122.1:c.311+115_311+117delinsCCT	ENSP00000493203.1:n.311+115_311+117delinsCCT
ENST00000389048.7:c.3515+115_3515+117delinsCCT	ENSP00000373700.3:n.3515+115_3515+117delinsCCT
ENST00000431873.5:c.395+115_395+117delinsCCT	ENSP00000414027.2:n.395+115_395+117delinsCCT
ENST00000453137.1:c.209+115_209+117delinsCCT	ENSP00000387488.1:n.209+115_209+117delinsCCT
ENST00000618119.4:c.2384+115_2384+117delinsCCT	ENSP00000482733.1:n.2384+115_2384+117delinsCCT
NM_004304.4:c.3515+115_3515+117delinsCCT	NP_004295.2:n.3515+115_3515+117delinsCCT
NM_001353765.1:c.311+115_311+117delinsCCT	NP_001340694.1:n.311+115_311+117delinsCCT
XM_024452778.1:c.668+115_668+117delinsCCT	XP_024308546.1:n.668+115_668+117delinsCCT
XM_024452779.1:c.311+115_311+117delinsCCT	XP_024308547.1:n.311+115_311+117delinsCCT
NM_004304.5:c.3515+115_3515+117delinsCCT MANE Select	NP_004295.2:n.3515+115_3515+117delinsCCT
NM_001353765.2:c.311+115_311+117delinsCCT	NP_001340694.1:n.311+115_311+117delinsCCT