Canonical Allele Identifier: CA645528799
Gene: ALK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29220748_29220749delinsTT , CM000664.2:g.29220748_29220749delinsTT GRCh38
NC_000002.11:g.29443614_29443615delinsTT , CM000664.1:g.29443614_29443615delinsTT GRCh37
NC_000002.10:g.29297118_29297119delinsTT NCBI36
NG_009445.1:g.705818_705819delinsAA , LRG_488:g.705818_705819delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3602_3603delinsAA MANE Select ENSP00000373700.3:p.Gly1201Glu
ENST00000431873.6:c.829_830delinsAA
ENST00000638605.1:n.479_480delinsAA
ENST00000642122.1:c.398_399delinsAA ENSP00000493203.1:p.Gly133Glu
ENST00000389048.7:c.3602_3603delinsAA ENSP00000373700.3:p.Gly1201Glu
ENST00000431873.5:c.482_483delinsAA ENSP00000414027.2:p.Gly161Glu
ENST00000618119.4:c.2471_2472delinsAA ENSP00000482733.1:p.Gly824Glu
NM_004304.4:c.3602_3603delinsAA NP_004295.2:p.Gly1201Glu
NM_001353765.1:c.398_399delinsAA NP_001340694.1:p.Gly133Glu
XM_024452778.1:c.755_756delinsAA XP_024308546.1:p.Gly252Glu
XM_024452779.1:c.398_399delinsAA XP_024308547.1:p.Gly133Glu
NM_004304.5:c.3602_3603delinsAA MANE Select NP_004295.2:p.Gly1201Glu
NM_001353765.2:c.398_399delinsAA NP_001340694.1:p.Gly133Glu