Canonical Allele Identifier: CA346469649

Gene: ALK

Linked Data

• dbSNP Id: rs1669415629
• MyVariant Identifiers: chr2:g.29432686T>C (hg19) ; chr2:g.29209820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209820T>C , CM000664.2:g.29209820T>C	GRCh38
NC_000002.11:g.29432686T>C , CM000664.1:g.29432686T>C	GRCh37
NC_000002.10:g.29286190T>C	NCBI36
NG_009445.1:g.716747A>G , LRG_488:g.716747A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3802A>G MANE Select	ENSP00000373700.3:p.Ile1268Val
ENST00000431873.6:c.1029A>G
ENST00000638605.1:n.679A>G
ENST00000642122.1:c.598A>G	ENSP00000493203.1:p.Ile200Val
ENST00000389048.7:c.3802A>G	ENSP00000373700.3:p.Ile1268Val
ENST00000431873.5:c.682A>G	ENSP00000414027.2:p.Ile228Val
ENST00000618119.4:c.2671A>G	ENSP00000482733.1:p.Ile891Val
NM_004304.4:c.3802A>G	NP_004295.2:p.Ile1268Val
NM_001353765.1:c.598A>G	NP_001340694.1:p.Ile200Val
XM_024452778.1:c.955A>G	XP_024308546.1:p.Ile319Val
XM_024452779.1:c.598A>G	XP_024308547.1:p.Ile200Val
NM_004304.5:c.3802A>G MANE Select	NP_004295.2:p.Ile1268Val
NM_001353765.2:c.598A>G	NP_001340694.1:p.Ile200Val