Canonical Allele Identifier: CA3250144360
Community Standard Title: NM_004304.5(ALK):c.4587_4596delinsGAGGGGTAAT (p.Asp1529Glu)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29193491_29193500delinsATTACCCCTC , CM000664.2:g.29193491_29193500delinsATTACCCCTC GRCh38
NC_000002.11:g.29416357_29416366delinsATTACCCCTC , CM000664.1:g.29416357_29416366delinsATTACCCCTC GRCh37
NC_000002.10:g.29269861_29269870delinsATTACCCCTC NCBI36
NG_009445.1:g.733067_733076delinsGAGGGGTAAT , LRG_488:g.733067_733076delinsGAGGGGTAAT

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.4587_4596delinsGAGGGGTAAT (ALK) MANE Select NP_004295.2:p.Asp1529Glu
ENST00000389048.8:c.4587_4596delinsGAGGGGTAAT (ALK) MANE Select ENSP00000373700.3:p.Asp1529Glu
NM_001353765.1:c.1383_1392delinsGAGGGGTAAT (ALK) NP_001340694.1:p.Asp461Glu
NM_001353765.2:c.1383_1392delinsGAGGGGTAAT (ALK) NP_001340694.1:p.Asp461Glu
NM_004304.4:c.4587_4596delinsGAGGGGTAAT (ALK) NP_004295.2:p.Asp1529Glu
ENST00000389048.7:c.4587_4596delinsGAGGGGTAAT (ALK) ENSP00000373700.3:p.Asp1529Glu
ENST00000431873.5:c.1467_1476delinsGAGGGGTAAT (ALK) ENSP00000414027.2:p.Asp489Glu
ENST00000431873.6:c.1814_1823delinsGAGGGGTAAT (ALK)
ENST00000618119.4:c.3456_3465delinsGAGGGGTAAT (ALK) ENSP00000482733.1:p.Asp1152Glu
ENST00000638605.1:n.1464_1473delinsGAGGGGTAAT (ALK)
ENST00000642122.1:c.1383_1392delinsGAGGGGTAAT (ALK) ENSP00000493203.1:p.Asp461Glu
ENST00000689605.1:c.1923-3437_1923-3428delinsATTACCCCTC (CLIP4) ENSP00000508948.1:n.1923-3437_1923-3428delinsATTACCCCTC
XM_024452778.1:c.1740_1749delinsGAGGGGTAAT (ALK) XP_024308546.1:p.Asp580Glu
XM_024452779.1:c.1383_1392delinsGAGGGGTAAT (ALK) XP_024308547.1:p.Asp461Glu