Canonical Allele Identifier: CA346463007

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445229T>C (hg19) ; chr2:g.29222363T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222363T>C , CM000664.2:g.29222363T>C	GRCh38
NC_000002.11:g.29445229T>C , CM000664.1:g.29445229T>C	GRCh37
NC_000002.10:g.29298733T>C	NCBI36
NG_009445.1:g.704204A>G , LRG_488:g.704204A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3496A>G MANE Select	ENSP00000373700.3:p.Met1166Val
ENST00000431873.6:c.723A>G
ENST00000638605.1:n.373A>G
ENST00000642122.1:c.292A>G	ENSP00000493203.1:p.Met98Val
ENST00000389048.7:c.3496A>G	ENSP00000373700.3:p.Met1166Val
ENST00000431873.5:c.376A>G	ENSP00000414027.2:p.Met126Val
ENST00000453137.1:c.190A>G	ENSP00000387488.1:p.Met64Val
ENST00000618119.4:c.2365A>G	ENSP00000482733.1:p.Met789Val
NM_004304.4:c.3496A>G	NP_004295.2:p.Met1166Val
NM_001353765.1:c.292A>G	NP_001340694.1:p.Met98Val
XM_024452778.1:c.649A>G	XP_024308546.1:p.Met217Val
XM_024452779.1:c.292A>G	XP_024308547.1:p.Met98Val
NM_004304.5:c.3496A>G MANE Select	NP_004295.2:p.Met1166Val
NM_001353765.2:c.292A>G	NP_001340694.1:p.Met98Val