Canonical Allele Identifier: CA767561855

Gene: ALK

Linked Data

• dbSNP Id: rs1248957314
• MyVariant Identifiers: chr2:g.29551755T>G (hg19) ; chr2:g.29328889T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328889T>G , CM000664.2:g.29328889T>G	GRCh38
NC_000002.11:g.29551755T>G , CM000664.1:g.29551755T>G	GRCh37
NC_000002.10:g.29405259T>G	NCBI36
NG_009445.1:g.597678A>C , LRG_488:g.597678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1283-408A>C MANE Select	ENSP00000373700.3:n.1283-408A>C
ENST00000389048.7:c.1283-408A>C	ENSP00000373700.3:n.1283-408A>C
ENST00000618119.4:c.152-408A>C	ENSP00000482733.1:n.152-408A>C
NM_004304.4:c.1283-408A>C	NP_004295.2:n.1283-408A>C
XR_939920.1:n.818-36T>G
XR_939921.1:n.680+6361T>G
XR_001738688.2:n.2213-408A>C
XR_939920.2:n.708-36T>G
XR_939921.2:n.576+6361T>G
NM_004304.5:c.1283-408A>C MANE Select	NP_004295.2:n.1283-408A>C