Canonical Allele Identifier: CA1241090506
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222345T= , CM000664.2:g.29222345T= GRCh38
NC_000002.11:g.29445211T= , CM000664.1:g.29445211T= GRCh37
NC_000002.10:g.29298715T= NCBI36
NG_009445.1:g.704222A= , LRG_488:g.704222A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3514A= MANE Select ENSP00000373700.3:p.Ser1172=
ENST00000431873.6:c.741A=
ENST00000638605.1:n.391A=
ENST00000642122.1:c.310A= ENSP00000493203.1:p.Ser104=
ENST00000389048.7:c.3514A= ENSP00000373700.3:p.Ser1172=
ENST00000431873.5:c.394A= ENSP00000414027.2:p.Ser132=
ENST00000453137.1:c.208A= ENSP00000387488.1:p.Ser70=
ENST00000618119.4:c.2383A= ENSP00000482733.1:p.Ser795=
NM_004304.4:c.3514A= NP_004295.2:p.Ser1172=
NM_001353765.1:c.310A= NP_001340694.1:p.Ser104=
XM_024452778.1:c.667A= XP_024308546.1:p.Ser223=
XM_024452779.1:c.310A= XP_024308547.1:p.Ser104=
NM_004304.5:c.3514A= MANE Select NP_004295.2:p.Ser1172=
NM_001353765.2:c.310A= NP_001340694.1:p.Ser104=