Canonical Allele Identifier: CA2201204574

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681545_681569delinsCACCAGGAGAGCGAGCTGCACTCCT , CM000678.2:g.681545_681569delinsCACCAGGAGAGCGAGCTGCACTCCT GRCh38
NC_000016.9:g.731545_731569delinsCACCAGGAGAGCGAGCTGCACTCCT , CM000678.1:g.731545_731569delinsCACCAGGAGAGCGAGCTGCACTCCT GRCh37
NC_000016.8:g.671546_671570delinsCACCAGGAGAGCGAGCTGCACTCCT NCBI36
NG_034141.1:g.6435_6459delinsCACCAGGAGAGCGAGCTGCACTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.466_490delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) MANE Select ENSP00000219548.4:p.His156=
ENST00000219548.8:c.466_490delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) ENSP00000219548.4:p.His156=
ENST00000563505.5:n.562_586delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1)
ENST00000564316.1:c.65_89delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1)
ENST00000564370.5:c.250_274delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) ENSP00000456875.1:p.His84=
ENST00000565677.5:c.250_274delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) ENSP00000457228.1:p.His84=
ENST00000566181.2:n.235_259delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1)
ENST00000566408.5:c.183_207delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1)
ENST00000567173.5:c.409_433delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) ENSP00000456591.1:p.His137=
ENST00000569248.5:n.1040_1064delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1)
ENST00000620831.4:c.-50+38242_-50+38266delinsCACCAGGAGAGCGAGCTGCACTCCT (MSLN) ENSP00000482893.1:n.-50+38242_-50+38266delinsCACCAGGAGAGCGAGC...
NM_001293197.1:c.250_274delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) NP_001280126.1:p.His84=
NM_005861.3:c.466_490delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) NP_005852.2:p.His156=
NM_005861.4:c.466_490delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) MANE Select NP_005852.2:p.His156=
NM_001293197.2:c.250_274delinsCACCAGGAGAGCGAGCTGCACTCCT (STUB1) NP_001280126.1:p.His84=