Canonical Allele Identifier: CA346473006

Gene: ALK

Linked Data

• ClinVar Variation Id: 2011294
• ClinVar RCV Id: RCV002851242
• dbSNP Id: rs2148166394
• MyVariant Identifiers: chr2:g.29443603T>C (hg19) ; chr2:g.29220737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220737T>C , CM000664.2:g.29220737T>C	GRCh38
NC_000002.11:g.29443603T>C , CM000664.1:g.29443603T>C	GRCh37
NC_000002.10:g.29297107T>C	NCBI36
NG_009445.1:g.705830A>G , LRG_488:g.705830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3614A>G MANE Select	ENSP00000373700.3:p.Lys1205Arg
ENST00000431873.6:c.841A>G
ENST00000638605.1:n.491A>G
ENST00000642122.1:c.410A>G	ENSP00000493203.1:p.Lys137Arg
ENST00000389048.7:c.3614A>G	ENSP00000373700.3:p.Lys1205Arg
ENST00000431873.5:c.494A>G	ENSP00000414027.2:p.Lys165Arg
ENST00000618119.4:c.2483A>G	ENSP00000482733.1:p.Lys828Arg
NM_004304.4:c.3614A>G	NP_004295.2:p.Lys1205Arg
NM_001353765.1:c.410A>G	NP_001340694.1:p.Lys137Arg
XM_024452778.1:c.767A>G	XP_024308546.1:p.Lys256Arg
XM_024452779.1:c.410A>G	XP_024308547.1:p.Lys137Arg
NM_004304.5:c.3614A>G MANE Select	NP_004295.2:p.Lys1205Arg
NM_001353765.2:c.410A>G	NP_001340694.1:p.Lys137Arg