Canonical Allele Identifier: CA767561834

Gene: ALK

Linked Data

• dbSNP Id: rs1338262663
• gnomAD v3: 2-29328773-CG-C
• gnomAD v4: 2-29328773-CG-C
• MyVariant Identifiers: chr2:g.29551640del (hg19) ; chr2:g.29328774del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328778del , CM000664.2:g.29328778del	GRCh38
NC_000002.11:g.29551644del , CM000664.1:g.29551644del	GRCh37
NC_000002.10:g.29405148del	NCBI36
NG_009445.1:g.597793del , LRG_488:g.597793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1283-293del MANE Select	ENSP00000373700.3:n.1283-293del
ENST00000389048.7:c.1283-293del	ENSP00000373700.3:n.1283-293del
ENST00000618119.4:c.152-293del	ENSP00000482733.1:n.152-293del
NM_004304.4:c.1283-293del	NP_004295.2:n.1283-293del
XR_939920.1:n.818-147del
XR_939921.1:n.680+6250del
XR_001738688.2:n.2213-293del
XR_939920.2:n.708-147del
XR_939921.2:n.576+6250del
NM_004304.5:c.1283-293del MANE Select	NP_004295.2:n.1283-293del