Canonical Allele Identifier: CA2739274309

Gene: ALK

Linked Data

• ClinVar Variation Id: 2811902
• ClinVar RCV Id: RCV003634652

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328502_29328503del , CM000664.2:g.29328502_29328503del	GRCh38
NC_000002.11:g.29551368_29551369del , CM000664.1:g.29551368_29551369del	GRCh37
NC_000002.10:g.29404872_29404873del	NCBI36
NG_009445.1:g.598069_598070del , LRG_488:g.598069_598070del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1283-17_1283-16del MANE Select	ENSP00000373700.3:n.1283-17_1283-16del
ENST00000389048.7:c.1283-17_1283-16del	ENSP00000373700.3:n.1283-17_1283-16del
ENST00000618119.4:c.152-17_152-16del	ENSP00000482733.1:n.152-17_152-16del
NM_004304.4:c.1283-17_1283-16del	NP_004295.2:n.1283-17_1283-16del
XR_939920.1:n.810_811del
XR_939921.1:n.680+5974_680+5975del
XR_001738688.2:n.2213-17_2213-16del
XR_939920.2:n.700_701del
XR_939921.2:n.576+5974_576+5975del
NM_004304.5:c.1283-17_1283-16del MANE Select	NP_004295.2:n.1283-17_1283-16del