Canonical Allele Identifier: CA2536653302
Gene: CNR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88163155_88163163del , CM000668.2:g.88163155_88163163del GRCh38
NC_000006.11:g.88872874_88872882del , CM000668.1:g.88872874_88872882del GRCh37
NC_000006.10:g.88929593_88929601del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.3:c.-64+1095_-64+1103del ENSP00000358511.2:n.-64+1095_-64+1103del
ENST00000369501.3:c.-64+2641_-64+2649del MANE Select ENSP00000358513.2:n.-64+2641_-64+2649del
ENST00000551417.2:c.-207+1095_-207+1103del ENSP00000446702.2:n.-207+1095_-207+1103de...
ENST00000369499.2:c.-64+1095_-64+1103del ENSP00000358511.2:n.-64+1095_-64+1103del
ENST00000369501.2:c.-64+2641_-64+2649del ENSP00000358513.2:n.-64+2641_-64+2649del
ENST00000551417.1:c.-207+1095_-207+1103del ENSP00000446702.1:n.-207+1095_-207+1103de...
NM_001160226.1:c.-207+2641_-207+2649del NP_001153698.1:n.-207+2641_-207+2649del
NM_001160258.1:c.-207+1095_-207+1103del NP_001153730.1:n.-207+1095_-207+1103del
NM_001160259.1:c.-64+2585_-64+2593del NP_001153731.1:n.-64+2585_-64+2593del
NM_016083.4:c.-64+2641_-64+2649del NP_057167.2:n.-64+2641_-64+2649del
XM_006715330.2:c.-64+3414_-64+3422del XP_006715393.1:n.-64+3414_-64+3422del
XM_011535424.1:c.-255+2641_-255+2649del XP_011533726.1:n.-255+2641_-255+2649del
XM_011535425.1:c.-255+1095_-255+1103del XP_011533727.1:n.-255+1095_-255+1103del
XM_011535426.1:c.-413+1095_-413+1103del XP_011533728.1:n.-413+1095_-413+1103del
XM_011535427.1:c.-366+1095_-366+1103del XP_011533729.1:n.-366+1095_-366+1103del
XM_011535428.1:c.-64+1095_-64+1103del XP_011533730.1:n.-64+1095_-64+1103del
NM_001160226.2:c.-207+2641_-207+2649del NP_001153698.1:n.-207+2641_-207+2649del
NM_001160258.2:c.-207+1095_-207+1103del NP_001153730.1:n.-207+1095_-207+1103del
NM_001160259.2:c.-64+2585_-64+2593del NP_001153731.1:n.-64+2585_-64+2593del
NM_001365869.1:c.-64+1095_-64+1103del NP_001352798.1:n.-64+1095_-64+1103del
NM_001365870.1:c.-255+2641_-255+2649del NP_001352799.1:n.-255+2641_-255+2649del
NM_001365872.1:c.-413+1095_-413+1103del NP_001352801.1:n.-413+1095_-413+1103del
NM_016083.5:c.-64+2641_-64+2649del NP_057167.2:n.-64+2641_-64+2649del
XM_006715330.3:c.-64+3414_-64+3422del XP_006715393.1:n.-64+3414_-64+3422del
XM_011535425.2:c.-255+1095_-255+1103del XP_011533727.1:n.-255+1095_-255+1103del
XM_017010240.2:c.-64+4028_-64+4036del XP_016865729.1:n.-64+4028_-64+4036del
NM_001160226.3:c.-207+2641_-207+2649del NP_001153698.1:n.-207+2641_-207+2649del
NM_001160258.3:c.-207+1095_-207+1103del NP_001153730.1:n.-207+1095_-207+1103del
NM_001160259.3:c.-64+2585_-64+2593del NP_001153731.1:n.-64+2585_-64+2593del
NM_001365869.2:c.-64+1095_-64+1103del NP_001352798.1:n.-64+1095_-64+1103del
NM_001365870.2:c.-255+2641_-255+2649del NP_001352799.1:n.-255+2641_-255+2649del
NM_001365872.2:c.-413+1095_-413+1103del NP_001352801.1:n.-413+1095_-413+1103del
NM_001370545.1:c.-64+3414_-64+3422del NP_001357474.1:n.-64+3414_-64+3422del
NM_001370546.1:c.-64+4028_-64+4036del NP_001357475.1:n.-64+4028_-64+4036del
NM_001370547.1:c.-255+1095_-255+1103del NP_001357476.1:n.-255+1095_-255+1103del
NM_016083.6:c.-64+2641_-64+2649del MANE Select NP_057167.2:n.-64+2641_-64+2649del