Canonical Allele Identifier: CA346463205
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 961489
ClinVar RCV Id: RCV001235187
dbSNP Id: rs749951867

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222387C>T , CM000664.2:g.29222387C>T GRCh38
NC_000002.11:g.29445253C>T , CM000664.1:g.29445253C>T GRCh37
NC_000002.10:g.29298757C>T NCBI36
NG_009445.1:g.704180G>A , LRG_488:g.704180G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3472G>A MANE Select ENSP00000373700.3:p.Glu1158Lys
ENST00000431873.6:c.699G>A
ENST00000638605.1:n.349G>A
ENST00000642122.1:c.268G>A ENSP00000493203.1:p.Glu90Lys
ENST00000389048.7:c.3472G>A ENSP00000373700.3:p.Glu1158Lys
ENST00000431873.5:c.352G>A ENSP00000414027.2:p.Glu118Lys
ENST00000453137.1:c.166G>A ENSP00000387488.1:p.Glu56Lys
ENST00000618119.4:c.2341G>A ENSP00000482733.1:p.Glu781Lys
NM_004304.4:c.3472G>A NP_004295.2:p.Glu1158Lys
NM_001353765.1:c.268G>A NP_001340694.1:p.Glu90Lys
XM_024452778.1:c.625G>A XP_024308546.1:p.Glu209Lys
XM_024452779.1:c.268G>A XP_024308547.1:p.Glu90Lys
NM_004304.5:c.3472G>A MANE Select NP_004295.2:p.Glu1158Lys
NM_001353765.2:c.268G>A NP_001340694.1:p.Glu90Lys