Canonical Allele Identifier: CA346462908

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445217T>C (hg19) ; chr2:g.29222351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222351T>C , CM000664.2:g.29222351T>C	GRCh38
NC_000002.11:g.29445217T>C , CM000664.1:g.29445217T>C	GRCh37
NC_000002.10:g.29298721T>C	NCBI36
NG_009445.1:g.704216A>G , LRG_488:g.704216A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3508A>G MANE Select	ENSP00000373700.3:p.Ile1170Val
ENST00000431873.6:c.735A>G
ENST00000638605.1:n.385A>G
ENST00000642122.1:c.304A>G	ENSP00000493203.1:p.Ile102Val
ENST00000389048.7:c.3508A>G	ENSP00000373700.3:p.Ile1170Val
ENST00000431873.5:c.388A>G	ENSP00000414027.2:p.Ile130Val
ENST00000453137.1:c.202A>G	ENSP00000387488.1:p.Ile68Val
ENST00000618119.4:c.2377A>G	ENSP00000482733.1:p.Ile793Val
NM_004304.4:c.3508A>G	NP_004295.2:p.Ile1170Val
NM_001353765.1:c.304A>G	NP_001340694.1:p.Ile102Val
XM_024452778.1:c.661A>G	XP_024308546.1:p.Ile221Val
XM_024452779.1:c.304A>G	XP_024308547.1:p.Ile102Val
NM_004304.5:c.3508A>G MANE Select	NP_004295.2:p.Ile1170Val
NM_001353765.2:c.304A>G	NP_001340694.1:p.Ile102Val