Canonical Allele Identifier: CA1241075089

Linked Data

dbSNP Id: rs1669050496

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29197461_29197464del , CM000664.2:g.29197461_29197464del GRCh38
NC_000002.11:g.29420327_29420330del , CM000664.1:g.29420327_29420330del GRCh37
NC_000002.10:g.29273831_29273834del NCBI36
NG_009445.1:g.729105_729108del , LRG_488:g.729105_729108del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689605.1:c.*455_*458del (CLIP4) ENSP00000508948.1:n.*455_*458del
ENST00000389048.8:c.4073+80_4073+83del (ALK) MANE Select ENSP00000373700.3:n.4073+80_4073+83del
ENST00000431873.6:c.1300+80_1300+83del (ALK)
ENST00000638605.1:n.950+80_950+83del (ALK)
ENST00000642122.1:c.869+80_869+83del (ALK) ENSP00000493203.1:n.869+80_869+83del
ENST00000389048.7:c.4073+80_4073+83del (ALK) ENSP00000373700.3:n.4073+80_4073+83del
ENST00000431873.5:c.953+80_953+83del (ALK) ENSP00000414027.2:n.953+80_953+83del
ENST00000618119.4:c.2942+80_2942+83del (ALK) ENSP00000482733.1:n.2942+80_2942+83del
NM_004304.4:c.4073+80_4073+83del (ALK) NP_004295.2:n.4073+80_4073+83del
NM_001353765.1:c.869+80_869+83del (ALK) NP_001340694.1:n.869+80_869+83del
XM_024452778.1:c.1226+80_1226+83del (ALK) XP_024308546.1:n.1226+80_1226+83del
XM_024452779.1:c.869+80_869+83del (ALK) XP_024308547.1:n.869+80_869+83del
NM_004304.5:c.4073+80_4073+83del (ALK) MANE Select NP_004295.2:n.4073+80_4073+83del
NM_001353765.2:c.869+80_869+83del (ALK) NP_001340694.1:n.869+80_869+83del