Canonical Allele Identifier: CA346473060

Gene: ALK

Linked Data

• dbSNP Id: rs1669780202
• COSMIC: COSM1169447
• MyVariant Identifiers: chr2:g.29443630A>T (hg19) ; chr2:g.29220764A>T (hg38)
• CIViC: CA346473060

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220764A>T , CM000664.2:g.29220764A>T	GRCh38
NC_000002.11:g.29443630A>T , CM000664.1:g.29443630A>T	GRCh37
NC_000002.10:g.29297134A>T	NCBI36
NG_009445.1:g.705803T>A , LRG_488:g.705803T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3587T>A MANE Select	ENSP00000373700.3:p.Leu1196Gln
ENST00000431873.6:c.814T>A
ENST00000638605.1:n.464T>A
ENST00000642122.1:c.383T>A	ENSP00000493203.1:p.Leu128Gln
ENST00000389048.7:c.3587T>A	ENSP00000373700.3:p.Leu1196Gln
ENST00000431873.5:c.467T>A	ENSP00000414027.2:p.Leu156Gln
ENST00000618119.4:c.2456T>A	ENSP00000482733.1:p.Leu819Gln
NM_004304.4:c.3587T>A	NP_004295.2:p.Leu1196Gln
NM_001353765.1:c.383T>A	NP_001340694.1:p.Leu128Gln
XM_024452778.1:c.740T>A	XP_024308546.1:p.Leu247Gln
XM_024452779.1:c.383T>A	XP_024308547.1:p.Leu128Gln
NM_004304.5:c.3587T>A MANE Select	NP_004295.2:p.Leu1196Gln
NM_001353765.2:c.383T>A	NP_001340694.1:p.Leu128Gln