Canonical Allele Identifier: CA1644859336
Gene: CNR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88154895_88154898delinsAAGC , CM000668.2:g.88154895_88154898delinsAAGC GRCh38
NC_000006.11:g.88864614_88864617delinsAAGC , CM000668.1:g.88864614_88864617delinsAAGC GRCh37
NC_000006.10:g.88921333_88921336delinsAAGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.3:c.-64+9359_-64+9362delinsGCTT ENSP00000358511.2:n.-64+9359_-64+9362deli...
ENST00000369501.3:c.-63-9561_-63-9558delinsGCTT MANE Select ENSP00000358513.2:n.-63-9561_-63-9558deli...
ENST00000428600.3:c.-64+8059_-64+8062delinsGCTT ENSP00000412192.2:n.-64+8059_-64+8062deli...
ENST00000551417.2:c.-206-7092_-206-7089delinsGCTT ENSP00000446702.2:n.-206-7092_-206-7089de...
ENST00000369499.2:c.-64+9359_-64+9362delinsGCTT ENSP00000358511.2:n.-64+9359_-64+9362deli...
ENST00000369501.2:c.-63-9561_-63-9558delinsGCTT ENSP00000358513.2:n.-63-9561_-63-9558deli...
ENST00000428600.2:c.-64+8059_-64+8062delinsGCTT ENSP00000412192.2:n.-64+8059_-64+8062deli...
ENST00000551417.1:c.-206-7092_-206-7089delinsGCTT ENSP00000446702.1:n.-206-7092_-206-7089de...
NM_001160226.1:c.-206-7092_-206-7089delinsGCTT NP_001153698.1:n.-206-7092_-206-7089delin...
NM_001160258.1:c.-206-7092_-206-7089delinsGCTT NP_001153730.1:n.-206-7092_-206-7089delin...
NM_001160259.1:c.-63-9561_-63-9558delinsGCTT NP_001153731.1:n.-63-9561_-63-9558delinsG...
NM_016083.4:c.-63-9561_-63-9558delinsGCTT NP_057167.2:n.-63-9561_-63-9558delinsGCTT...
XM_006715330.2:c.-63-9561_-63-9558delinsGCTT XP_006715393.1:n.-63-9561_-63-9558delinsG...
XM_011535424.1:c.-254-7092_-254-7089delinsGCTT XP_011533726.1:n.-254-7092_-254-7089delin...
XM_011535425.1:c.-254-7092_-254-7089delinsGCTT XP_011533727.1:n.-254-7092_-254-7089delin...
XM_011535426.1:c.-412-4258_-412-4255delinsGCTT XP_011533728.1:n.-412-4258_-412-4255delin...
XM_011535427.1:c.-365-4305_-365-4302delinsGCTT XP_011533729.1:n.-365-4305_-365-4302delin...
XM_011535428.1:c.-64+9359_-64+9362delinsGCTT XP_011533730.1:n.-64+9359_-64+9362delinsG...
NM_001160226.2:c.-206-7092_-206-7089delinsGCTT NP_001153698.1:n.-206-7092_-206-7089delin...
NM_001160258.2:c.-206-7092_-206-7089delinsGCTT NP_001153730.1:n.-206-7092_-206-7089delin...
NM_001160259.2:c.-63-9561_-63-9558delinsGCTT NP_001153731.1:n.-63-9561_-63-9558delinsG...
NM_001365869.1:c.-64+9359_-64+9362delinsGCTT NP_001352798.1:n.-64+9359_-64+9362delinsG...
NM_001365870.1:c.-254-7092_-254-7089delinsGCTT NP_001352799.1:n.-254-7092_-254-7089delin...
NM_001365872.1:c.-412-4258_-412-4255delinsGCTT NP_001352801.1:n.-412-4258_-412-4255delin...
NM_001365874.1:c.-64+8059_-64+8062delinsGCTT NP_001352803.1:n.-64+8059_-64+8062delinsG...
NM_016083.5:c.-63-9561_-63-9558delinsGCTT NP_057167.2:n.-63-9561_-63-9558delinsGCTT...
XM_006715330.3:c.-63-9561_-63-9558delinsGCTT XP_006715393.1:n.-63-9561_-63-9558delinsG...
XM_011535425.2:c.-254-7092_-254-7089delinsGCTT XP_011533727.1:n.-254-7092_-254-7089delin...
XM_017010240.2:c.-63-9561_-63-9558delinsGCTT XP_016865729.1:n.-63-9561_-63-9558delinsG...
NM_001160226.3:c.-206-7092_-206-7089delinsGCTT NP_001153698.1:n.-206-7092_-206-7089delin...
NM_001160258.3:c.-206-7092_-206-7089delinsGCTT NP_001153730.1:n.-206-7092_-206-7089delin...
NM_001160259.3:c.-63-9561_-63-9558delinsGCTT NP_001153731.1:n.-63-9561_-63-9558delinsG...
NM_001365869.2:c.-64+9359_-64+9362delinsGCTT NP_001352798.1:n.-64+9359_-64+9362delinsG...
NM_001365870.2:c.-254-7092_-254-7089delinsGCTT NP_001352799.1:n.-254-7092_-254-7089delin...
NM_001365872.2:c.-412-4258_-412-4255delinsGCTT NP_001352801.1:n.-412-4258_-412-4255delin...
NM_001365874.2:c.-64+8059_-64+8062delinsGCTT NP_001352803.1:n.-64+8059_-64+8062delinsG...
NM_001370545.1:c.-63-9561_-63-9558delinsGCTT NP_001357474.1:n.-63-9561_-63-9558delinsG...
NM_001370546.1:c.-63-9561_-63-9558delinsGCTT NP_001357475.1:n.-63-9561_-63-9558delinsG...
NM_001370547.1:c.-254-7092_-254-7089delinsGCTT NP_001357476.1:n.-254-7092_-254-7089delin...
NM_016083.6:c.-63-9561_-63-9558delinsGCTT MANE Select NP_057167.2:n.-63-9561_-63-9558delinsGCTT...
NM_001365874.3:c.-64+8059_-64+8062delinsGCTT NP_001352803.1:n.-64+8059_-64+8062delinsG...