Canonical Allele Identifier: CA1644866137

Gene: CNR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163021_88163026delinsACTGAG , CM000668.2:g.88163021_88163026delinsACTGAG	GRCh38
NC_000006.11:g.88872740_88872745delinsACTGAG , CM000668.1:g.88872740_88872745delinsACTGAG	GRCh37
NC_000006.10:g.88929459_88929464delinsACTGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+1231_-64+1236delinsCTCAGT	ENSP00000358511.2:n.-64+1231_-64+1236delinsCTCAGT
ENST00000369501.3:c.-64+2777_-64+2782delinsCTCAGT MANE Select	ENSP00000358513.2:n.-64+2777_-64+2782delinsCTCAGT
ENST00000551417.2:c.-207+1231_-207+1236delinsCTCAGT	ENSP00000446702.2:n.-207+1231_-207+1236delinsCTCAGT
ENST00000369499.2:c.-64+1231_-64+1236delinsCTCAGT	ENSP00000358511.2:n.-64+1231_-64+1236delinsCTCAGT
ENST00000369501.2:c.-64+2777_-64+2782delinsCTCAGT	ENSP00000358513.2:n.-64+2777_-64+2782delinsCTCAGT
ENST00000551417.1:c.-207+1231_-207+1236delinsCTCAGT	ENSP00000446702.1:n.-207+1231_-207+1236delinsCTCAGT
NM_001160226.1:c.-207+2777_-207+2782delinsCTCAGT	NP_001153698.1:n.-207+2777_-207+2782delinsCTCAGT
NM_001160258.1:c.-207+1231_-207+1236delinsCTCAGT	NP_001153730.1:n.-207+1231_-207+1236delinsCTCAGT
NM_001160259.1:c.-64+2721_-64+2726delinsCTCAGT	NP_001153731.1:n.-64+2721_-64+2726delinsCTCAGT
NM_016083.4:c.-64+2777_-64+2782delinsCTCAGT	NP_057167.2:n.-64+2777_-64+2782delinsCTCAGT
XM_006715330.2:c.-64+3550_-64+3555delinsCTCAGT	XP_006715393.1:n.-64+3550_-64+3555delinsCTCAGT
XM_011535424.1:c.-255+2777_-255+2782delinsCTCAGT	XP_011533726.1:n.-255+2777_-255+2782delinsCTCAGT
XM_011535425.1:c.-255+1231_-255+1236delinsCTCAGT	XP_011533727.1:n.-255+1231_-255+1236delinsCTCAGT
XM_011535426.1:c.-413+1231_-413+1236delinsCTCAGT	XP_011533728.1:n.-413+1231_-413+1236delinsCTCAGT
XM_011535427.1:c.-366+1231_-366+1236delinsCTCAGT	XP_011533729.1:n.-366+1231_-366+1236delinsCTCAGT
XM_011535428.1:c.-64+1231_-64+1236delinsCTCAGT	XP_011533730.1:n.-64+1231_-64+1236delinsCTCAGT
NM_001160226.2:c.-207+2777_-207+2782delinsCTCAGT	NP_001153698.1:n.-207+2777_-207+2782delinsCTCAGT
NM_001160258.2:c.-207+1231_-207+1236delinsCTCAGT	NP_001153730.1:n.-207+1231_-207+1236delinsCTCAGT
NM_001160259.2:c.-64+2721_-64+2726delinsCTCAGT	NP_001153731.1:n.-64+2721_-64+2726delinsCTCAGT
NM_001365869.1:c.-64+1231_-64+1236delinsCTCAGT	NP_001352798.1:n.-64+1231_-64+1236delinsCTCAGT
NM_001365870.1:c.-255+2777_-255+2782delinsCTCAGT	NP_001352799.1:n.-255+2777_-255+2782delinsCTCAGT
NM_001365872.1:c.-413+1231_-413+1236delinsCTCAGT	NP_001352801.1:n.-413+1231_-413+1236delinsCTCAGT
NM_001365874.1:c.-133_-128delinsCTCAGT	NP_001352803.1:n.-133_-128delinsCTCAGT
NM_016083.5:c.-64+2777_-64+2782delinsCTCAGT	NP_057167.2:n.-64+2777_-64+2782delinsCTCAGT
XM_006715330.3:c.-64+3550_-64+3555delinsCTCAGT	XP_006715393.1:n.-64+3550_-64+3555delinsCTCAGT
XM_011535425.2:c.-255+1231_-255+1236delinsCTCAGT	XP_011533727.1:n.-255+1231_-255+1236delinsCTCAGT
XM_017010240.2:c.-64+4164_-64+4169delinsCTCAGT	XP_016865729.1:n.-64+4164_-64+4169delinsCTCAGT
NM_001160226.3:c.-207+2777_-207+2782delinsCTCAGT	NP_001153698.1:n.-207+2777_-207+2782delinsCTCAGT
NM_001160258.3:c.-207+1231_-207+1236delinsCTCAGT	NP_001153730.1:n.-207+1231_-207+1236delinsCTCAGT
NM_001160259.3:c.-64+2721_-64+2726delinsCTCAGT	NP_001153731.1:n.-64+2721_-64+2726delinsCTCAGT
NM_001365869.2:c.-64+1231_-64+1236delinsCTCAGT	NP_001352798.1:n.-64+1231_-64+1236delinsCTCAGT
NM_001365870.2:c.-255+2777_-255+2782delinsCTCAGT	NP_001352799.1:n.-255+2777_-255+2782delinsCTCAGT
NM_001365872.2:c.-413+1231_-413+1236delinsCTCAGT	NP_001352801.1:n.-413+1231_-413+1236delinsCTCAGT
NM_001370545.1:c.-64+3550_-64+3555delinsCTCAGT	NP_001357474.1:n.-64+3550_-64+3555delinsCTCAGT
NM_001370546.1:c.-64+4164_-64+4169delinsCTCAGT	NP_001357475.1:n.-64+4164_-64+4169delinsCTCAGT
NM_001370547.1:c.-255+1231_-255+1236delinsCTCAGT	NP_001357476.1:n.-255+1231_-255+1236delinsCTCAGT
NM_016083.6:c.-64+2777_-64+2782delinsCTCAGT MANE Select	NP_057167.2:n.-64+2777_-64+2782delinsCTCAGT