Canonical Allele Identifier: CA3061297298

Gene: CNR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163222_88163223insA , CM000668.2:g.88163222_88163223insA	GRCh38
NC_000006.11:g.88872941_88872942insA , CM000668.1:g.88872941_88872942insA	GRCh37
NC_000006.10:g.88929660_88929661insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369499.3:c.-64+1034_-64+1035insT	ENSP00000358511.2:n.-64+1034_-64+1035insT
ENST00000369501.3:c.-64+2580_-64+2581insT MANE Select	ENSP00000358513.2:n.-64+2580_-64+2581insT
ENST00000551417.2:c.-207+1034_-207+1035insT	ENSP00000446702.2:n.-207+1034_-207+1035insT
ENST00000369499.2:c.-64+1034_-64+1035insT	ENSP00000358511.2:n.-64+1034_-64+1035insT
ENST00000369501.2:c.-64+2580_-64+2581insT	ENSP00000358513.2:n.-64+2580_-64+2581insT
ENST00000551417.1:c.-207+1034_-207+1035insT	ENSP00000446702.1:n.-207+1034_-207+1035insT
NM_001160226.1:c.-207+2580_-207+2581insT	NP_001153698.1:n.-207+2580_-207+2581insT
NM_001160258.1:c.-207+1034_-207+1035insT	NP_001153730.1:n.-207+1034_-207+1035insT
NM_001160259.1:c.-64+2524_-64+2525insT	NP_001153731.1:n.-64+2524_-64+2525insT
NM_016083.4:c.-64+2580_-64+2581insT	NP_057167.2:n.-64+2580_-64+2581insT
XM_006715330.2:c.-64+3353_-64+3354insT	XP_006715393.1:n.-64+3353_-64+3354insT
XM_011535424.1:c.-255+2580_-255+2581insT	XP_011533726.1:n.-255+2580_-255+2581insT
XM_011535425.1:c.-255+1034_-255+1035insT	XP_011533727.1:n.-255+1034_-255+1035insT
XM_011535426.1:c.-413+1034_-413+1035insT	XP_011533728.1:n.-413+1034_-413+1035insT
XM_011535427.1:c.-366+1034_-366+1035insT	XP_011533729.1:n.-366+1034_-366+1035insT
XM_011535428.1:c.-64+1034_-64+1035insT	XP_011533730.1:n.-64+1034_-64+1035insT
NM_001160226.2:c.-207+2580_-207+2581insT	NP_001153698.1:n.-207+2580_-207+2581insT
NM_001160258.2:c.-207+1034_-207+1035insT	NP_001153730.1:n.-207+1034_-207+1035insT
NM_001160259.2:c.-64+2524_-64+2525insT	NP_001153731.1:n.-64+2524_-64+2525insT
NM_001365869.1:c.-64+1034_-64+1035insT	NP_001352798.1:n.-64+1034_-64+1035insT
NM_001365870.1:c.-255+2580_-255+2581insT	NP_001352799.1:n.-255+2580_-255+2581insT
NM_001365872.1:c.-413+1034_-413+1035insT	NP_001352801.1:n.-413+1034_-413+1035insT
NM_016083.5:c.-64+2580_-64+2581insT	NP_057167.2:n.-64+2580_-64+2581insT
XM_006715330.3:c.-64+3353_-64+3354insT	XP_006715393.1:n.-64+3353_-64+3354insT
XM_011535425.2:c.-255+1034_-255+1035insT	XP_011533727.1:n.-255+1034_-255+1035insT
XM_017010240.2:c.-64+3967_-64+3968insT	XP_016865729.1:n.-64+3967_-64+3968insT
NM_001160226.3:c.-207+2580_-207+2581insT	NP_001153698.1:n.-207+2580_-207+2581insT
NM_001160258.3:c.-207+1034_-207+1035insT	NP_001153730.1:n.-207+1034_-207+1035insT
NM_001160259.3:c.-64+2524_-64+2525insT	NP_001153731.1:n.-64+2524_-64+2525insT
NM_001365869.2:c.-64+1034_-64+1035insT	NP_001352798.1:n.-64+1034_-64+1035insT
NM_001365870.2:c.-255+2580_-255+2581insT	NP_001352799.1:n.-255+2580_-255+2581insT
NM_001365872.2:c.-413+1034_-413+1035insT	NP_001352801.1:n.-413+1034_-413+1035insT
NM_001370545.1:c.-64+3353_-64+3354insT	NP_001357474.1:n.-64+3353_-64+3354insT
NM_001370546.1:c.-64+3967_-64+3968insT	NP_001357475.1:n.-64+3967_-64+3968insT
NM_001370547.1:c.-255+1034_-255+1035insT	NP_001357476.1:n.-255+1034_-255+1035insT
NM_016083.6:c.-64+2580_-64+2581insT MANE Select	NP_057167.2:n.-64+2580_-64+2581insT