Canonical Allele Identifier: CA650548311

Gene: CNR1

Linked Data

• COSMIC: COSN16641241

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88148916_88148917insA , CM000668.2:g.88148916_88148917insA	GRCh38
NC_000006.11:g.88858635_88858636insA , CM000668.1:g.88858635_88858636insA	GRCh37
NC_000006.10:g.88915354_88915355insA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-63-3580_-63-3579insT	ENSP00000358511.2:n.-63-3580_-63-3579insT...
ENST00000369501.3:c.-63-3580_-63-3579insT MANE Select	ENSP00000358513.2:n.-63-3580_-63-3579insT...
ENST00000428600.3:c.-63-3580_-63-3579insT	ENSP00000412192.2:n.-63-3580_-63-3579insT...
ENST00000551417.2:c.-206-1111_-206-1110insT	ENSP00000446702.2:n.-206-1111_-206-1110in...
ENST00000369499.2:c.-63-3580_-63-3579insT	ENSP00000358511.2:n.-63-3580_-63-3579insT...
ENST00000369501.2:c.-63-3580_-63-3579insT	ENSP00000358513.2:n.-63-3580_-63-3579insT...
ENST00000428600.2:c.-63-3580_-63-3579insT	ENSP00000412192.2:n.-63-3580_-63-3579insT...
ENST00000551417.1:c.-206-1111_-206-1110insT	ENSP00000446702.1:n.-206-1111_-206-1110in...
NM_001160226.1:c.-206-1111_-206-1110insT	NP_001153698.1:n.-206-1111_-206-1110insT
NM_001160258.1:c.-206-1111_-206-1110insT	NP_001153730.1:n.-206-1111_-206-1110insT
NM_001160259.1:c.-63-3580_-63-3579insT	NP_001153731.1:n.-63-3580_-63-3579insT
NM_016083.4:c.-63-3580_-63-3579insT	NP_057167.2:n.-63-3580_-63-3579insT
XM_005248650.3:c.-254-1111_-254-1110insT	XP_005248707.1:n.-254-1111_-254-1110insT
XM_006715330.2:c.-63-3580_-63-3579insT	XP_006715393.1:n.-63-3580_-63-3579insT
XM_011535424.1:c.-254-1111_-254-1110insT	XP_011533726.1:n.-254-1111_-254-1110insT
XM_011535425.1:c.-254-1111_-254-1110insT	XP_011533727.1:n.-254-1111_-254-1110insT
XM_011535426.1:c.-254-1111_-254-1110insT	XP_011533728.1:n.-254-1111_-254-1110insT
XM_011535427.1:c.-254-1111_-254-1110insT	XP_011533729.1:n.-254-1111_-254-1110insT
XM_011535428.1:c.-63-3580_-63-3579insT	XP_011533730.1:n.-63-3580_-63-3579insT
NM_001160226.2:c.-206-1111_-206-1110insT	NP_001153698.1:n.-206-1111_-206-1110insT
NM_001160258.2:c.-206-1111_-206-1110insT	NP_001153730.1:n.-206-1111_-206-1110insT
NM_001160259.2:c.-63-3580_-63-3579insT	NP_001153731.1:n.-63-3580_-63-3579insT
NM_001365869.1:c.-63-3580_-63-3579insT	NP_001352798.1:n.-63-3580_-63-3579insT
NM_001365870.1:c.-254-1111_-254-1110insT	NP_001352799.1:n.-254-1111_-254-1110insT
NM_001365872.1:c.-254-1111_-254-1110insT	NP_001352801.1:n.-254-1111_-254-1110insT
NM_001365874.1:c.-63-3580_-63-3579insT	NP_001352803.1:n.-63-3580_-63-3579insT
NM_016083.5:c.-63-3580_-63-3579insT	NP_057167.2:n.-63-3580_-63-3579insT
XM_006715330.3:c.-63-3580_-63-3579insT	XP_006715393.1:n.-63-3580_-63-3579insT
XM_011535425.2:c.-254-1111_-254-1110insT	XP_011533727.1:n.-254-1111_-254-1110insT
XM_017010240.2:c.-63-3580_-63-3579insT	XP_016865729.1:n.-63-3580_-63-3579insT
NM_001160226.3:c.-206-1111_-206-1110insT	NP_001153698.1:n.-206-1111_-206-1110insT
NM_001160258.3:c.-206-1111_-206-1110insT	NP_001153730.1:n.-206-1111_-206-1110insT
NM_001160259.3:c.-63-3580_-63-3579insT	NP_001153731.1:n.-63-3580_-63-3579insT
NM_001365869.2:c.-63-3580_-63-3579insT	NP_001352798.1:n.-63-3580_-63-3579insT
NM_001365870.2:c.-254-1111_-254-1110insT	NP_001352799.1:n.-254-1111_-254-1110insT
NM_001365872.2:c.-254-1111_-254-1110insT	NP_001352801.1:n.-254-1111_-254-1110insT
NM_001365874.2:c.-63-3580_-63-3579insT	NP_001352803.1:n.-63-3580_-63-3579insT
NM_001370545.1:c.-63-3580_-63-3579insT	NP_001357474.1:n.-63-3580_-63-3579insT
NM_001370546.1:c.-63-3580_-63-3579insT	NP_001357475.1:n.-63-3580_-63-3579insT
NM_001370547.1:c.-254-1111_-254-1110insT	NP_001357476.1:n.-254-1111_-254-1110insT
NM_016083.6:c.-63-3580_-63-3579insT MANE Select	NP_057167.2:n.-63-3580_-63-3579insT
NM_001365874.3:c.-63-3580_-63-3579insT	NP_001352803.1:n.-63-3580_-63-3579insT