Canonical Allele Identifier: CA44665003

Gene: ALK

Linked Data

• dbSNP Id: rs564922778
• MyVariant Identifiers: chr2:g.29551545A>C (hg19) ; chr2:g.29328679A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328679A>C , CM000664.2:g.29328679A>C	GRCh38
NC_000002.11:g.29551545A>C , CM000664.1:g.29551545A>C	GRCh37
NC_000002.10:g.29405049A>C	NCBI36
NG_009445.1:g.597888T>G , LRG_488:g.597888T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1283-198T>G MANE Select	ENSP00000373700.3:n.1283-198T>G
ENST00000389048.7:c.1283-198T>G	ENSP00000373700.3:n.1283-198T>G
ENST00000618119.4:c.152-198T>G	ENSP00000482733.1:n.152-198T>G
NM_004304.4:c.1283-198T>G	NP_004295.2:n.1283-198T>G
XR_939920.1:n.817+170A>C
XR_939921.1:n.680+6151A>C
XR_001738688.2:n.2213-198T>G
XR_939920.2:n.707+170A>C
XR_939921.2:n.576+6151A>C
NM_004304.5:c.1283-198T>G MANE Select	NP_004295.2:n.1283-198T>G