Canonical Allele Identifier: CA1241090552
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222431_29222434delinsGGGA , CM000664.2:g.29222431_29222434delinsGGGA GRCh38
NC_000002.11:g.29445297_29445300delinsGGGA , CM000664.1:g.29445297_29445300delinsGGGA GRCh37
NC_000002.10:g.29298801_29298804delinsGGGA NCBI36
NG_009445.1:g.704133_704136delinsTCCC , LRG_488:g.704133_704136delinsTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3451-26_3451-23delinsTCCC MANE Select ENSP00000373700.3:n.3451-26_3451-23delinsTCCC
ENST00000431873.6:c.678-26_678-23delinsTCCC
ENST00000638605.1:n.328-26_328-23delinsTCCC
ENST00000642122.1:c.247-26_247-23delinsTCCC ENSP00000493203.1:n.247-26_247-23delinsTCCC
ENST00000389048.7:c.3451-26_3451-23delinsTCCC ENSP00000373700.3:n.3451-26_3451-23delinsTCCC
ENST00000431873.5:c.331-26_331-23delinsTCCC ENSP00000414027.2:n.331-26_331-23delinsTCCC
ENST00000453137.1:c.145-26_145-23delinsTCCC ENSP00000387488.1:n.145-26_145-23delinsTCCC
ENST00000618119.4:c.2320-26_2320-23delinsTCCC ENSP00000482733.1:n.2320-26_2320-23delinsTCCC
NM_004304.4:c.3451-26_3451-23delinsTCCC NP_004295.2:n.3451-26_3451-23delinsTCCC
NM_001353765.1:c.247-26_247-23delinsTCCC NP_001340694.1:n.247-26_247-23delinsTCCC
XM_024452778.1:c.604-26_604-23delinsTCCC XP_024308546.1:n.604-26_604-23delinsTCCC
XM_024452779.1:c.247-26_247-23delinsTCCC XP_024308547.1:n.247-26_247-23delinsTCCC
NM_004304.5:c.3451-26_3451-23delinsTCCC MANE Select NP_004295.2:n.3451-26_3451-23delinsTCCC
NM_001353765.2:c.247-26_247-23delinsTCCC NP_001340694.1:n.247-26_247-23delinsTCCC