Canonical Allele Identifier: CA2697547994

Gene: ALK

Linked Data

• ClinVar Variation Id: 2771500
• ClinVar RCV Id: RCV003517828

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222326_29222327del , CM000664.2:g.29222326_29222327del	GRCh38
NC_000002.11:g.29445192_29445193del , CM000664.1:g.29445192_29445193del	GRCh37
NC_000002.10:g.29298696_29298697del	NCBI36
NG_009445.1:g.704242_704243del , LRG_488:g.704242_704243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+19_3515+20del MANE Select	ENSP00000373700.3:n.3515+19_3515+20del
ENST00000431873.6:c.742+19_742+20del
ENST00000638605.1:n.392+19_392+20del
ENST00000642122.1:c.311+19_311+20del	ENSP00000493203.1:n.311+19_311+20del
ENST00000389048.7:c.3515+19_3515+20del	ENSP00000373700.3:n.3515+19_3515+20del
ENST00000431873.5:c.395+19_395+20del	ENSP00000414027.2:n.395+19_395+20del
ENST00000453137.1:c.209+19_209+20del	ENSP00000387488.1:n.209+19_209+20del
ENST00000618119.4:c.2384+19_2384+20del	ENSP00000482733.1:n.2384+19_2384+20del
NM_004304.4:c.3515+19_3515+20del	NP_004295.2:n.3515+19_3515+20del
NM_001353765.1:c.311+19_311+20del	NP_001340694.1:n.311+19_311+20del
XM_024452778.1:c.668+19_668+20del	XP_024308546.1:n.668+19_668+20del
XM_024452779.1:c.311+19_311+20del	XP_024308547.1:n.311+19_311+20del
NM_004304.5:c.3515+19_3515+20del MANE Select	NP_004295.2:n.3515+19_3515+20del
NM_001353765.2:c.311+19_311+20del	NP_001340694.1:n.311+19_311+20del