Canonical Allele Identifier: CA1241074863

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29197248_29197253delinsGGGACT , CM000664.2:g.29197248_29197253delinsGGGACT GRCh38
NC_000002.11:g.29420114_29420119delinsGGGACT , CM000664.1:g.29420114_29420119delinsGGGACT GRCh37
NC_000002.10:g.29273618_29273623delinsGGGACT NCBI36
NG_009445.1:g.729314_729319delinsAGTCCC , LRG_488:g.729314_729319delinsAGTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000689605.1:c.*242_*247delinsGGGACT (CLIP4) ENSP00000508948.1:n.*242_*247delinsGGGACT
ENST00000389048.8:c.4073+289_4073+294delinsAGTCCC (ALK) MANE Select ENSP00000373700.3:n.4073+289_4073+294delinsAGTCCC
ENST00000431873.6:c.1300+289_1300+294delinsAGTCCC (ALK)
ENST00000638605.1:n.950+289_950+294delinsAGTCCC (ALK)
ENST00000642122.1:c.869+289_869+294delinsAGTCCC (ALK) ENSP00000493203.1:n.869+289_869+294delinsAGTCCC
ENST00000389048.7:c.4073+289_4073+294delinsAGTCCC (ALK) ENSP00000373700.3:n.4073+289_4073+294delinsAGTCCC
ENST00000431873.5:c.953+289_953+294delinsAGTCCC (ALK) ENSP00000414027.2:n.953+289_953+294delinsAGTCCC
ENST00000618119.4:c.2942+289_2942+294delinsAGTCCC (ALK) ENSP00000482733.1:n.2942+289_2942+294delinsAGTCCC
NM_004304.4:c.4073+289_4073+294delinsAGTCCC (ALK) NP_004295.2:n.4073+289_4073+294delinsAGTCCC
NM_001353765.1:c.869+289_869+294delinsAGTCCC (ALK) NP_001340694.1:n.869+289_869+294delinsAGTCCC
XM_024452778.1:c.1226+289_1226+294delinsAGTCCC (ALK) XP_024308546.1:n.1226+289_1226+294delinsAGTCCC
XM_024452779.1:c.869+289_869+294delinsAGTCCC (ALK) XP_024308547.1:n.869+289_869+294delinsAGTCCC
NM_004304.5:c.4073+289_4073+294delinsAGTCCC (ALK) MANE Select NP_004295.2:n.4073+289_4073+294delinsAGTCCC
NM_001353765.2:c.869+289_869+294delinsAGTCCC (ALK) NP_001340694.1:n.869+289_869+294delinsAGTCCC