Canonical Allele Identifier: CA3031432076
Gene: CNR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88163236_88163237insAGTATATATTGCGTAATTTTGGACACCT , CM000668.2:g.88163236_88163237insAGTATATATTGCGTAATTTTGGACACCT GRCh38
NC_000006.11:g.88872955_88872956insAGTATATATTGCGTAATTTTGGACACCT , CM000668.1:g.88872955_88872956insAGTATATATTGCGTAATTTTGGACACCT GRCh37
NC_000006.10:g.88929674_88929675insAGTATATATTGCGTAATTTTGGACACCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369499.3:c.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATATACT ENSP00000358511.2:n.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAAT...
ENST00000369501.3:c.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATACT MANE Select ENSP00000358513.2:n.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAAT...
ENST00000551417.2:c.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATATATACT ENSP00000446702.2:n.-207+1020_-207+1021insAGGTGTCCAAAATTACGCA...
ENST00000369499.2:c.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATATACT ENSP00000358511.2:n.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAAT...
ENST00000369501.2:c.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATACT ENSP00000358513.2:n.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAAT...
ENST00000551417.1:c.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATATATACT ENSP00000446702.1:n.-207+1020_-207+1021insAGGTGTCCAAAATTACGCA...
NM_001160226.1:c.-207+2566_-207+2567insAGGTGTCCAAAATTACGCAATATATACT NP_001153698.1:n.-207+2566_-207+2567insAGGTGTCCAAAATTACGCAATA...
NM_001160258.1:c.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001153730.1:n.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATA...
NM_001160259.1:c.-64+2510_-64+2511insAGGTGTCCAAAATTACGCAATATATACT NP_001153731.1:n.-64+2510_-64+2511insAGGTGTCCAAAATTACGCAATATA...
NM_016083.4:c.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATACT NP_057167.2:n.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATAC...
XM_006715330.2:c.-64+3339_-64+3340insAGGTGTCCAAAATTACGCAATATATACT XP_006715393.1:n.-64+3339_-64+3340insAGGTGTCCAAAATTACGCAATATA...
XM_011535424.1:c.-255+2566_-255+2567insAGGTGTCCAAAATTACGCAATATATACT XP_011533726.1:n.-255+2566_-255+2567insAGGTGTCCAAAATTACGCAATA...
XM_011535425.1:c.-255+1020_-255+1021insAGGTGTCCAAAATTACGCAATATATACT XP_011533727.1:n.-255+1020_-255+1021insAGGTGTCCAAAATTACGCAATA...
XM_011535426.1:c.-413+1020_-413+1021insAGGTGTCCAAAATTACGCAATATATACT XP_011533728.1:n.-413+1020_-413+1021insAGGTGTCCAAAATTACGCAATA...
XM_011535427.1:c.-366+1020_-366+1021insAGGTGTCCAAAATTACGCAATATATACT XP_011533729.1:n.-366+1020_-366+1021insAGGTGTCCAAAATTACGCAATA...
XM_011535428.1:c.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATATACT XP_011533730.1:n.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATA...
NM_001160226.2:c.-207+2566_-207+2567insAGGTGTCCAAAATTACGCAATATATACT NP_001153698.1:n.-207+2566_-207+2567insAGGTGTCCAAAATTACGCAATA...
NM_001160258.2:c.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001153730.1:n.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATA...
NM_001160259.2:c.-64+2510_-64+2511insAGGTGTCCAAAATTACGCAATATATACT NP_001153731.1:n.-64+2510_-64+2511insAGGTGTCCAAAATTACGCAATATA...
NM_001365869.1:c.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001352798.1:n.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATA...
NM_001365870.1:c.-255+2566_-255+2567insAGGTGTCCAAAATTACGCAATATATACT NP_001352799.1:n.-255+2566_-255+2567insAGGTGTCCAAAATTACGCAATA...
NM_001365872.1:c.-413+1020_-413+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001352801.1:n.-413+1020_-413+1021insAGGTGTCCAAAATTACGCAATA...
NM_016083.5:c.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATACT NP_057167.2:n.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATAC...
XM_006715330.3:c.-64+3339_-64+3340insAGGTGTCCAAAATTACGCAATATATACT XP_006715393.1:n.-64+3339_-64+3340insAGGTGTCCAAAATTACGCAATATA...
XM_011535425.2:c.-255+1020_-255+1021insAGGTGTCCAAAATTACGCAATATATACT XP_011533727.1:n.-255+1020_-255+1021insAGGTGTCCAAAATTACGCAATA...
XM_017010240.2:c.-64+3953_-64+3954insAGGTGTCCAAAATTACGCAATATATACT XP_016865729.1:n.-64+3953_-64+3954insAGGTGTCCAAAATTACGCAATATA...
NM_001160226.3:c.-207+2566_-207+2567insAGGTGTCCAAAATTACGCAATATATACT NP_001153698.1:n.-207+2566_-207+2567insAGGTGTCCAAAATTACGCAATA...
NM_001160258.3:c.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001153730.1:n.-207+1020_-207+1021insAGGTGTCCAAAATTACGCAATA...
NM_001160259.3:c.-64+2510_-64+2511insAGGTGTCCAAAATTACGCAATATATACT NP_001153731.1:n.-64+2510_-64+2511insAGGTGTCCAAAATTACGCAATATA...
NM_001365869.2:c.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001352798.1:n.-64+1020_-64+1021insAGGTGTCCAAAATTACGCAATATA...
NM_001365870.2:c.-255+2566_-255+2567insAGGTGTCCAAAATTACGCAATATATACT NP_001352799.1:n.-255+2566_-255+2567insAGGTGTCCAAAATTACGCAATA...
NM_001365872.2:c.-413+1020_-413+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001352801.1:n.-413+1020_-413+1021insAGGTGTCCAAAATTACGCAATA...
NM_001370545.1:c.-64+3339_-64+3340insAGGTGTCCAAAATTACGCAATATATACT NP_001357474.1:n.-64+3339_-64+3340insAGGTGTCCAAAATTACGCAATATA...
NM_001370546.1:c.-64+3953_-64+3954insAGGTGTCCAAAATTACGCAATATATACT NP_001357475.1:n.-64+3953_-64+3954insAGGTGTCCAAAATTACGCAATATA...
NM_001370547.1:c.-255+1020_-255+1021insAGGTGTCCAAAATTACGCAATATATACT NP_001357476.1:n.-255+1020_-255+1021insAGGTGTCCAAAATTACGCAATA...
NM_016083.6:c.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATACT MANE Select NP_057167.2:n.-64+2566_-64+2567insAGGTGTCCAAAATTACGCAATATATAC...