Canonical Allele Identifier: CA425434580

Gene: ALK

Linked Data

• dbSNP Id: rs1228794467
• MyVariant Identifiers: chr2:g.29445251T>C (hg19) ; chr2:g.29222385T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222385T>C , CM000664.2:g.29222385T>C	GRCh38
NC_000002.11:g.29445251T>C , CM000664.1:g.29445251T>C	GRCh37
NC_000002.10:g.29298755T>C	NCBI36
NG_009445.1:g.704182A>G , LRG_488:g.704182A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3474A>G MANE Select	ENSP00000373700.3:p.Glu1158=
ENST00000431873.6:c.701A>G
ENST00000638605.1:n.351A>G
ENST00000642122.1:c.270A>G	ENSP00000493203.1:p.Glu90=
ENST00000389048.7:c.3474A>G	ENSP00000373700.3:p.Glu1158=
ENST00000431873.5:c.354A>G	ENSP00000414027.2:p.Glu118=
ENST00000453137.1:c.168A>G	ENSP00000387488.1:p.Glu56=
ENST00000618119.4:c.2343A>G	ENSP00000482733.1:p.Glu781=
NM_004304.4:c.3474A>G	NP_004295.2:p.Glu1158=
NM_001353765.1:c.270A>G	NP_001340694.1:p.Glu90=
XM_024452778.1:c.627A>G	XP_024308546.1:p.Glu209=
XM_024452779.1:c.270A>G	XP_024308547.1:p.Glu90=
NM_004304.5:c.3474A>G MANE Select	NP_004295.2:p.Glu1158=
NM_001353765.2:c.270A>G	NP_001340694.1:p.Glu90=