Canonical Allele Identifier: CA2576925456

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29197691del , CM000664.2:g.29197691del GRCh38
NC_000002.11:g.29420557del , CM000664.1:g.29420557del GRCh37
NC_000002.10:g.29274061del NCBI36
NG_009445.1:g.728876del , LRG_488:g.728876del

Transcript Alleles

HGVS Amino-acid change
ENST00000689605.1:c.*685del (CLIP4) ENSP00000508948.1:n.*685del
ENST00000389048.8:c.3939-15del (ALK) MANE Select ENSP00000373700.3:n.3939-15del
ENST00000431873.6:c.1166-15del (ALK)
ENST00000638605.1:n.816-15del (ALK)
ENST00000642122.1:c.735-15del (ALK) ENSP00000493203.1:n.735-15del
ENST00000389048.7:c.3939-15del (ALK) ENSP00000373700.3:n.3939-15del
ENST00000431873.5:c.819-15del (ALK) ENSP00000414027.2:n.819-15del
ENST00000618119.4:c.2808-15del (ALK) ENSP00000482733.1:n.2808-15del
NM_004304.4:c.3939-15del (ALK) NP_004295.2:n.3939-15del
NM_001353765.1:c.735-15del (ALK) NP_001340694.1:n.735-15del
XM_024452778.1:c.1092-15del (ALK) XP_024308546.1:n.1092-15del
XM_024452779.1:c.735-15del (ALK) XP_024308547.1:n.735-15del
NM_004304.5:c.3939-15del (ALK) MANE Select NP_004295.2:n.3939-15del
NM_001353765.2:c.735-15del (ALK) NP_001340694.1:n.735-15del