Canonical Allele Identifier: CA346469646

Gene: ALK

Linked Data

• COSMIC: COSM1244838
• MyVariant Identifiers: chr2:g.29432685A>C (hg19) ; chr2:g.29209819A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209819A>C , CM000664.2:g.29209819A>C	GRCh38
NC_000002.11:g.29432685A>C , CM000664.1:g.29432685A>C	GRCh37
NC_000002.10:g.29286189A>C	NCBI36
NG_009445.1:g.716748T>G , LRG_488:g.716748T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3803T>G MANE Select	ENSP00000373700.3:p.Ile1268Ser
ENST00000431873.6:c.1030T>G
ENST00000638605.1:n.680T>G
ENST00000642122.1:c.599T>G	ENSP00000493203.1:p.Ile200Ser
ENST00000389048.7:c.3803T>G	ENSP00000373700.3:p.Ile1268Ser
ENST00000431873.5:c.683T>G	ENSP00000414027.2:p.Ile228Ser
ENST00000618119.4:c.2672T>G	ENSP00000482733.1:p.Ile891Ser
NM_004304.4:c.3803T>G	NP_004295.2:p.Ile1268Ser
NM_001353765.1:c.599T>G	NP_001340694.1:p.Ile200Ser
XM_024452778.1:c.956T>G	XP_024308546.1:p.Ile319Ser
XM_024452779.1:c.599T>G	XP_024308547.1:p.Ile200Ser
NM_004304.5:c.3803T>G MANE Select	NP_004295.2:p.Ile1268Ser
NM_001353765.2:c.599T>G	NP_001340694.1:p.Ile200Ser