Canonical Allele Identifier: CA346462896

Gene: ALK

Linked Data

• COSMIC: COSM98477
• MyVariant Identifiers: chr2:g.29445216A>C (hg19) ; chr2:g.29222350A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222350A>C , CM000664.2:g.29222350A>C	GRCh38
NC_000002.11:g.29445216A>C , CM000664.1:g.29445216A>C	GRCh37
NC_000002.10:g.29298720A>C	NCBI36
NG_009445.1:g.704217T>G , LRG_488:g.704217T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3509T>G MANE Select	ENSP00000373700.3:p.Ile1170Ser
ENST00000431873.6:c.736T>G
ENST00000638605.1:n.386T>G
ENST00000642122.1:c.305T>G	ENSP00000493203.1:p.Ile102Ser
ENST00000389048.7:c.3509T>G	ENSP00000373700.3:p.Ile1170Ser
ENST00000431873.5:c.389T>G	ENSP00000414027.2:p.Ile130Ser
ENST00000453137.1:c.203T>G	ENSP00000387488.1:p.Ile68Ser
ENST00000618119.4:c.2378T>G	ENSP00000482733.1:p.Ile793Ser
NM_004304.4:c.3509T>G	NP_004295.2:p.Ile1170Ser
NM_001353765.1:c.305T>G	NP_001340694.1:p.Ile102Ser
XM_024452778.1:c.662T>G	XP_024308546.1:p.Ile221Ser
XM_024452779.1:c.305T>G	XP_024308547.1:p.Ile102Ser
NM_004304.5:c.3509T>G MANE Select	NP_004295.2:p.Ile1170Ser
NM_001353765.2:c.305T>G	NP_001340694.1:p.Ile102Ser