Canonical Allele Identifier: CA2679637049

Gene: CNR1

Linked Data

• gnomAD v4: 6-88163117-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163118_88163119insAGC , CM000668.2:g.88163118_88163119insAGC	GRCh38
NC_000006.11:g.88872837_88872838insAGC , CM000668.1:g.88872837_88872838insAGC	GRCh37
NC_000006.10:g.88929556_88929557insAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+1139_-64+1140insCTG	ENSP00000358511.2:n.-64+1139_-64+1140insC...
ENST00000369501.3:c.-64+2685_-64+2686insCTG MANE Select	ENSP00000358513.2:n.-64+2685_-64+2686insC...
ENST00000551417.2:c.-207+1139_-207+1140insCTG	ENSP00000446702.2:n.-207+1139_-207+1140in...
ENST00000369499.2:c.-64+1139_-64+1140insCTG	ENSP00000358511.2:n.-64+1139_-64+1140insC...
ENST00000369501.2:c.-64+2685_-64+2686insCTG	ENSP00000358513.2:n.-64+2685_-64+2686insC...
ENST00000551417.1:c.-207+1139_-207+1140insCTG	ENSP00000446702.1:n.-207+1139_-207+1140in...
NM_001160226.1:c.-207+2685_-207+2686insCTG	NP_001153698.1:n.-207+2685_-207+2686insCT...
NM_001160258.1:c.-207+1139_-207+1140insCTG	NP_001153730.1:n.-207+1139_-207+1140insCT...
NM_001160259.1:c.-64+2629_-64+2630insCTG	NP_001153731.1:n.-64+2629_-64+2630insCTG
NM_016083.4:c.-64+2685_-64+2686insCTG	NP_057167.2:n.-64+2685_-64+2686insCTG
XM_006715330.2:c.-64+3458_-64+3459insCTG	XP_006715393.1:n.-64+3458_-64+3459insCTG
XM_011535424.1:c.-255+2685_-255+2686insCTG	XP_011533726.1:n.-255+2685_-255+2686insCT...
XM_011535425.1:c.-255+1139_-255+1140insCTG	XP_011533727.1:n.-255+1139_-255+1140insCT...
XM_011535426.1:c.-413+1139_-413+1140insCTG	XP_011533728.1:n.-413+1139_-413+1140insCT...
XM_011535427.1:c.-366+1139_-366+1140insCTG	XP_011533729.1:n.-366+1139_-366+1140insCT...
XM_011535428.1:c.-64+1139_-64+1140insCTG	XP_011533730.1:n.-64+1139_-64+1140insCTG
NM_001160226.2:c.-207+2685_-207+2686insCTG	NP_001153698.1:n.-207+2685_-207+2686insCT...
NM_001160258.2:c.-207+1139_-207+1140insCTG	NP_001153730.1:n.-207+1139_-207+1140insCT...
NM_001160259.2:c.-64+2629_-64+2630insCTG	NP_001153731.1:n.-64+2629_-64+2630insCTG
NM_001365869.1:c.-64+1139_-64+1140insCTG	NP_001352798.1:n.-64+1139_-64+1140insCTG
NM_001365870.1:c.-255+2685_-255+2686insCTG	NP_001352799.1:n.-255+2685_-255+2686insCT...
NM_001365872.1:c.-413+1139_-413+1140insCTG	NP_001352801.1:n.-413+1139_-413+1140insCT...
NM_016083.5:c.-64+2685_-64+2686insCTG	NP_057167.2:n.-64+2685_-64+2686insCTG
XM_006715330.3:c.-64+3458_-64+3459insCTG	XP_006715393.1:n.-64+3458_-64+3459insCTG
XM_011535425.2:c.-255+1139_-255+1140insCTG	XP_011533727.1:n.-255+1139_-255+1140insCT...
XM_017010240.2:c.-64+4072_-64+4073insCTG	XP_016865729.1:n.-64+4072_-64+4073insCTG
NM_001160226.3:c.-207+2685_-207+2686insCTG	NP_001153698.1:n.-207+2685_-207+2686insCT...
NM_001160258.3:c.-207+1139_-207+1140insCTG	NP_001153730.1:n.-207+1139_-207+1140insCT...
NM_001160259.3:c.-64+2629_-64+2630insCTG	NP_001153731.1:n.-64+2629_-64+2630insCTG
NM_001365869.2:c.-64+1139_-64+1140insCTG	NP_001352798.1:n.-64+1139_-64+1140insCTG
NM_001365870.2:c.-255+2685_-255+2686insCTG	NP_001352799.1:n.-255+2685_-255+2686insCT...
NM_001365872.2:c.-413+1139_-413+1140insCTG	NP_001352801.1:n.-413+1139_-413+1140insCT...
NM_001370545.1:c.-64+3458_-64+3459insCTG	NP_001357474.1:n.-64+3458_-64+3459insCTG
NM_001370546.1:c.-64+4072_-64+4073insCTG	NP_001357475.1:n.-64+4072_-64+4073insCTG
NM_001370547.1:c.-255+1139_-255+1140insCTG	NP_001357476.1:n.-255+1139_-255+1140insCT...
NM_016083.6:c.-64+2685_-64+2686insCTG MANE Select	NP_057167.2:n.-64+2685_-64+2686insCTG