Canonical Allele Identifier: CA2739274310

Gene: ALK

Linked Data

• ClinVar Variation Id: 2829571
• ClinVar RCV Id: RCV003634914

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328498C>G , CM000664.2:g.29328498C>G	GRCh38
NC_000002.11:g.29551364C>G , CM000664.1:g.29551364C>G	GRCh37
NC_000002.10:g.29404868C>G	NCBI36
NG_009445.1:g.598069G>C , LRG_488:g.598069G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1283-17G>C MANE Select	ENSP00000373700.3:n.1283-17G>C
ENST00000389048.7:c.1283-17G>C	ENSP00000373700.3:n.1283-17G>C
ENST00000618119.4:c.152-17G>C	ENSP00000482733.1:n.152-17G>C
NM_004304.4:c.1283-17G>C	NP_004295.2:n.1283-17G>C
XR_939920.1:n.806C>G
XR_939921.1:n.680+5970C>G
XR_001738688.2:n.2213-17G>C
XR_939920.2:n.696C>G
XR_939921.2:n.576+5970C>G
NM_004304.5:c.1283-17G>C MANE Select	NP_004295.2:n.1283-17G>C